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Rodan LH, Spillmann RC, Kurata HT, et al. Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations. Genet Med. 2021;23(10):2016doi: 10.1038/s41436-021-01306-7.
Rodan, L. H., Spillmann, R. C., Kurata, H. T., Lamothe, S. M., Maghera, J., Jamra, R. A., Alkelai, A., Antonarakis, S. E., Atallah, I., Bar-Yosef, O., Bilan, F., Bjorgo, K., Blanc, X., Van Bogaert, P., Bolkier, Y., Burrage, L. C., Christ, B. U., Granadillo, J. L., Dickson, P., Donald, K. A., Dubourg, C., Eliyahu, A., Emrick, L., Engleman, K., Gonfiantini, M. V., Good, J. M., Kalser, J., Kloeckner, C., Lachmeijer, G., Macchiaiolo, M., Nicita, F., Odent, S., O'Heir, E., Ortiz-Gonzalez, X., Pacio-Miguez, M., Palomares-Bralo, M., Pena, L., Platzer, K., Quinodoz, M., Ranza, E., Rosenfeld, J. A., Roulet-Perez, E., Santani, A., Santos-Simarro, F., Pode-Shakked, B., Skraban, C., Slaugh, R., Superti-Furga, A., Thiffault, I., van Jaabrsveld, R. H., Vincent, M., Wang, H. G., Zacher, P., Rush, E., Pitt, G. S., Au, P. Y. B., & Shashi, V. (2021). Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations. Genetics in medicine : official journal of the American College of Medical Genetics, 23(10), 2016. https://doi.org/10.1038/s41436-021-01306-7
Rodan, Lance H, et al. "Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations." Genetics in medicine : official journal of the American College of Medical Genetics vol. 23,10 (2021): 2016. doi: https://doi.org/10.1038/s41436-021-01306-7
Rodan LH, Spillmann RC, Kurata HT, Lamothe SM, Maghera J, Jamra RA, Alkelai A, Antonarakis SE, Atallah I, Bar-Yosef O, Bilan F, Bjorgo K, Blanc X, Van Bogaert P, Bolkier Y, Burrage LC, Christ BU, Granadillo JL, Dickson P, Donald KA, Dubourg C, Eliyahu A, Emrick L, Engleman K, Gonfiantini MV, Good JM, Kalser J, Kloeckner C, Lachmeijer G, Macchiaiolo M, Nicita F, Odent S, O'Heir E, Ortiz-Gonzalez X, Pacio-Miguez M, Palomares-Bralo M, Pena L, Platzer K, Quinodoz M, Ranza E, Rosenfeld JA, Roulet-Perez E, Santani A, Santos-Simarro F, Pode-Shakked B, Skraban C, Slaugh R, Superti-Furga A, Thiffault I, van Jaabrsveld RH, Vincent M, Wang HG, Zacher P, Rush E, Pitt GS, Au PYB, Shashi V. Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations. Genet Med. 2021 Oct;23(10):2016. doi: 10.1038/s41436-021-01306-7. PMID: 34522029.
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Genet Med. 2021 Oct;23(10):2016. doi: 10.1038/s41436-021-01306-7.

Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations.

Genetics in medicine : official journal of the American College of Medical Genetics

Lance H Rodan, Rebecca C Spillmann, Harley T Kurata, Shawn M Lamothe, Jasmine Maghera, Rami Abou Jamra, Anna Alkelai, Stylianos E Antonarakis, Isis Atallah, Omer Bar-Yosef, Frédéric Bilan, Kathrine Bjorgo, Xavier Blanc, Patrick Van Bogaert, Yoav Bolkier, Lindsay C Burrage, Björn U Christ, Jorge L Granadillo, Patricia Dickson, Kirsten A Donald, Christèle Dubourg, Aviva Eliyahu, Lisa Emrick, Kendra Engleman, Michaela Veronika Gonfiantini, Jean-Marc Good, Judith Kalser, Chiara Kloeckner, Guus Lachmeijer, Marina Macchiaiolo, Francesco Nicita, Sylvie Odent, Emily O'Heir, Xilma Ortiz-Gonzalez, Marta Pacio-Miguez, María Palomares-Bralo, Loren Pena, Konrad Platzer, Mathieu Quinodoz, Emmanuelle Ranza, Jill A Rosenfeld, Eliane Roulet-Perez, Avni Santani, Fernando Santos-Simarro, Ben Pode-Shakked, Cara Skraban, Rachel Slaugh, Andrea Superti-Furga, Isabelle Thiffault, Richard H van Jaabrsveld, Marie Vincent, Hong-Gang Wang, Pia Zacher, Eric Rush, Geoffrey S Pitt, Ping Yee Billie Au, Vandana Shashi

Affiliations

  1. Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.
  2. Department of Neurology, Boston Children's Hospital, Boston, MA, USA.
  3. Division of Medical Genetics, Department of Pediatrics, Duke Health, Durham, NC, USA.
  4. Department of Pharmacology, Alberta Diabetes Institute, University of Alberta, Edmonton, AB, Canada.
  5. Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
  6. Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA.
  7. Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.
  8. Division of Genetic Medicine, Lausanne University Hospital, Lausanne, Switzerland.
  9. Pediatric Neurology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hahsomer, Israel.
  10. Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  11. CHU de Poitiers, Service de Génétique, EA3808 NEUVACOD, Poitiers, France.
  12. Department of Medical Genetics, Oslo University Hospital, Oslo, Norway.
  13. CHU d'Angers, Service de Pédiatrie, EA3808 NEUVACOD, Angers, France.
  14. Pediatric Cardiology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hahsomer, Israel.
  15. Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  16. Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Cape Town, SA, South Africa.
  17. Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.
  18. Service de Génétique Moléculaire et Génomique, CHU, Rennes, France.
  19. University of Rennes, CNRS, IGDR, UMR 6290, Rennes, France.
  20. The Danek Gertner Insitute of Human Genetics, Sheba Medical Center, Tel-Hahsomer, Israel.
  21. Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hahsomer, Israel.
  22. Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO, USA.
  23. Rare Diseases and Medical Genetic Unit, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
  24. Pediatric Neurology, Lausanne University Hospital, Lausanne, Switzerland.
  25. Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  26. Unit of Neuromuscular and Neurodegenerative Diseases, Department of Neurosciences and Neurorehabilitation, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
  27. Service de Génétique Clinique, Centre de référence "Maladies Rares" Anomalies du développement CLAD-Ouest, Hôpital SUD, Échirolles, France.
  28. Center for Mendelian Genomics and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  29. Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  30. Instituto de Genética Médica y Molecular (INGEMM), Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.
  31. Cincinnati Children's Hospital and Medical Center Cincinnati, Cincinnati, OH, USA.
  32. University of Cincinnati College of Medicine Cincinnati, Cincinnati, OH, USA.
  33. Institute of Molecular and Clinical Ophthalmology Basel (IOB), Basel, Switzerland.
  34. Department of Ophthalmology, University of Basel, Basel, Switzerland.
  35. Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  36. Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
  37. Institute of Rare Diseases, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hahsomer, Israel.
  38. Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  39. Service de Génétique Médicale, CHU Nantes, France; Inserm, CNRS, Univ Nantes, l'institut du thorax, Nantes, France.
  40. Cardiovascular Research Institute, Weill Cornell Medicine, New York, NY, USA.
  41. The Saxon Epilepsy Center Kleinwachau, Radeberg, Germany.
  42. The Children's Mercy Hospital, Kansas City, MO, USA.
  43. Department of Pediatrics University of Missouri-Kansas City, Kansas City, MO, USA.
  44. Department of Internal Medicine, University of Kansas Medical Center, Kansas City, MO, USA.
  45. Alberta Children's Hospital Research Institute, Department of Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
  46. Division of Medical Genetics, Department of Pediatrics, Duke Health, Durham, NC, USA. [email protected].

PMID: 34522029 DOI: 10.1038/s41436-021-01306-7

[No abstract available.]

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