MT‐CYB mutations in hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

MT‐CYB mutations in hypertrophic cardiomyopathy

Published:2013-04-12 Issue:1 Volume:1 Page:54-65
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Hagen Christian M.¹²,Aidt Frederik H.¹³,Havndrup Ole⁴,Hedley Paula L.¹⁵,Jespersgaard Cathrine¹,Jensen Morten⁶,Kanters Jørgen K.²,Moolman‐Smook Johanna C.⁵,Møller Daniel V.¹,Bundgaard Henning⁶,Christiansen Michael¹

Affiliation:

1. Department of Clinical Biochemistry, Immunology, and Genetics Statens Serum Institut Copenhagen Denmark

2. Department of Biomedical Sciences University of Copenhagen Copenhagen Denmark

3. Institute of Cellular and Molecular Medicine Faculty of Health Sciences University of Copenhagen Copenhagen Denmark

4. Department of Cardiology Roskilde Sygehus Roskilde Denmark

5. Department of Biomedical Sciences Stellenbosch University Cape Town South Africa

6. Department of Medicine B The Heart Center Rigshospitalet Copenhagen Denmark

Funder

Lundbeckfonden

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.5

Reference50 articles.

1. Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives

2. A Missense Mutation in the Mitochondrial Cytochrome b Gene in a Revisited Case with Histiocytoid Cardiomyopathy

3. Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure

4. Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations

5. The Dawn of Human Matrilineal Diversity

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