Mitochondrial Haplogroups Modify the Risk of Developing Hypertrophic Cardiomyopathy in a Danish Population

Hypertrophic cardiomyopathy (HCM) is a genetic disorder caused by mutations in genes coding for proteins involved in sarcomere function. The disease is associated with mitochondrial dysfunction. Evolutionarily developed variation in mitochondrial DNA (mtDNA), defining mtDNA haplogroups and haplogrou...

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Detalhes bibliográficos
Main Authors: Hagen, Christian M., Aidt, Frederik H., Hedley, Paula L., Jensen, Morten K., Havndrup, Ole, Kanters, Jørgen K., Moolman-Smook, Johanna C., Larsen, Severin O., Bundgaard, Henning, Christiansen, Michael
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3734310/
https://ncbi.nlm.nih.gov/pubmed/23940792
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0071904
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