Private Mitochondrial DNA Variants in Danish Patients with Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is a genetic cardiac disease primarily caused by mutations in genes coding for sarcomeric proteins. A molecular-genetic etiology can be established in ~60% of cases. Evolutionarily conserved mitochondrial DNA (mtDNA) haplogroups are susceptibility factors for HCM. S...

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Detalles Bibliográficos
Autores principales: Hagen, Christian M., Aidt, Frederik H., Havndrup, Ole, Hedley, Paula L., Jensen, Morten K., Kanters, Jørgen K., Pham, Tam T., Bundgaard, Henning, Christiansen, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414448/
https://www.ncbi.nlm.nih.gov/pubmed/25923817
http://dx.doi.org/10.1371/journal.pone.0124540

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414448/
https://www.ncbi.nlm.nih.gov/pubmed/25923817
http://dx.doi.org/10.1371/journal.pone.0124540

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