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David D, Almeida LS, Maggi M, et al. Clinical Severity of PGK1 Deficiency Due To a Novel p.E120K Substitution Is Exacerbated by Co-inheritance of a Subclinical Translocation t(3;14)(q26.33;q12), Disrupting NUBPL Gene. JIMD Rep. 2015;23:55-65doi: 10.1007/8904_2015_427.
David, D., Almeida, L. S., Maggi, M., Araújo, C., Imreh, S., Valentini, G., Fekete, G., & Haltrich, I. (2015). Clinical Severity of PGK1 Deficiency Due To a Novel p.E120K Substitution Is Exacerbated by Co-inheritance of a Subclinical Translocation t(3;14)(q26.33;q12), Disrupting NUBPL Gene. JIMD reports, 2355-65. https://doi.org/10.1007/8904_2015_427
David, Dezső, et al. "Clinical Severity of PGK1 Deficiency Due To a Novel p.E120K Substitution Is Exacerbated by Co-inheritance of a Subclinical Translocation t(3;14)(q26.33;q12), Disrupting NUBPL Gene." JIMD reports vol. 23 (2015): 55-65. doi: https://doi.org/10.1007/8904_2015_427
David D, Almeida LS, Maggi M, Araújo C, Imreh S, Valentini G, Fekete G, Haltrich I. Clinical Severity of PGK1 Deficiency Due To a Novel p.E120K Substitution Is Exacerbated by Co-inheritance of a Subclinical Translocation t(3;14)(q26.33;q12), Disrupting NUBPL Gene. JIMD Rep. 2015;23:55-65. doi: 10.1007/8904_2015_427. Epub 2015 Mar 27. PMID: 25814383; PMCID: PMC4484905.
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