MT-CYB mutations in hypertrophic cardiomyopathy

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Mitochondrial dysfunction is a characteristic of heart failure. Mutations in mitochondrial DNA, particularly in MT-CYB coding for cytochrome B in complex III (CIII), have been associated with isolated hypertrophic cardiomyopathy (HCM). We hypothesized that MT-CYB mutations might play an important ca...

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Detalles Bibliográficos
Autores principales: Hagen, Christian M, Aidt, Frederik H, Havndrup, Ole, Hedley, Paula L, Jespersgaard, Cathrine, Jensen, Morten, Kanters, Jørgen K, Moolman-Smook, Johanna C, Møller, Daniel V, Bundgaard, Henning, Christiansen, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893158/
https://www.ncbi.nlm.nih.gov/pubmed/24498601
http://dx.doi.org/10.1002/mgg3.5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893158/
https://www.ncbi.nlm.nih.gov/pubmed/24498601
http://dx.doi.org/10.1002/mgg3.5

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