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Heliö K, Mäyränpää MI, Saarinen I, et al. GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy. Front Genet. 2021;12:786705doi: 10.3389/fgene.2021.786705.
Heliö, K., Mäyränpää, M. I., Saarinen, I., Ahonen, S., Junnila, H., Tommiska, J., Weckström, S., Holmström, M., Toivonen, M., Nikus, K., Hathaway, J., Siivonen, P., Muona, M., Sistonen, J., Salmenperä, P., Gentile, M., Paananen, J., Myllykangas, S., Alastalo, T. P., Heliö, T., & Koskenvuo, J. (2021). GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy. Frontiers in genetics, 12786705. https://doi.org/10.3389/fgene.2021.786705
Heliö, Krista, et al. "GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy." Frontiers in genetics vol. 12 (2021): 786705. doi: https://doi.org/10.3389/fgene.2021.786705
Heliö K, Mäyränpää MI, Saarinen I, Ahonen S, Junnila H, Tommiska J, Weckström S, Holmström M, Toivonen M, Nikus K, Hathaway J, Siivonen P, Muona M, Sistonen J, Salmenperä P, Gentile M, Paananen J, Myllykangas S, Alastalo TP, Heliö T, Koskenvuo J. GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy. Front Genet. 2021 Nov 25;12:786705. doi: 10.3389/fgene.2021.786705. eCollection 2021. PMID: 34899865; PMCID: PMC8656111.
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Front Genet. 2021 Nov 25;12:786705. doi: 10.3389/fgene.2021.786705. eCollection 2021.

GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy.

Frontiers in genetics

Krista Heliö, Mikko I Mäyränpää, Inka Saarinen, Saija Ahonen, Heidi Junnila, Johanna Tommiska, Sini Weckström, Miia Holmström, Mia Toivonen, Kjell Nikus, Julie Hathaway, Pauli Siivonen, Mikko Muona, Johanna Sistonen, Pertteli Salmenperä, Massimiliano Gentile, Jussi Paananen, Samuel Myllykangas, Tero-Pekka Alastalo, Tiina Heliö, Juha Koskenvuo

Affiliations

  1. Heart and Lung Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
  2. Department of Pathology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
  3. Blueprint Genetics, A Quest Diagnostics Company, Espoo, Finland.
  4. Department of Radiology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
  5. Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
  6. Heart Center, Tampere University Hospital, Tampere, Finland.

PMID: 34899865 PMCID: PMC8656111 DOI: 10.3389/fgene.2021.786705

[No abstract available.]

Copyright © 2021 Heliö, Mäyränpää, Saarinen, Ahonen, Junnila, Tommiska, Weckström, Holmström, Toivonen, Nikus, Hathaway, Siivonen, Muona, Sistonen, Salmenperä, Gentile, Paananen, Myllykangas, Alastalo, Heliö and Koskenvuo.

Keywords: GCOM1; MYZAP; autosomal recessive; cardiomyopathy; dilated cardiomyopathy

Conflict of interest statement

Authors IS, SA, HJ, JT, MT, JH, PS, MMU, JS, PS, MG, JP, SM, T-PA, and JK were employed by the company Blueprint Genetics, A Quest Diagnostics Company. The remaining authors declare that the research

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