Genetic, clinical, molecular, and pathogenic aspects of the South Asian–specific polymorphic MYBPC3(Δ25bp) variant

Hypertrophic cardiomyopathy (HCM) is a cardiac genetic disease characterized by ventricular enlargement, diastolic dysfunction, and increased risk for sudden cardiac death. Sarcomeric genetic defects are the predominant known cause of HCM. In particular, mutations in the myosin-binding protein C gen...

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Библиографические подробности
Опубликовано в: :Biophys Rev
Главные авторы: Arif, Mohammed, Nabavizadeh, Pooneh, Song, Taejeong, Desai, Darshini, Singh, Rohit, Bazrafshan, Sholeh, Kumar, Mohit, Wang, Yigang, Gilbert, Richard J., Dhandapany, Perundurai S., Becker, Richard C., Kranias, Evangelia G., Sadayappan, Sakthivel
Формат: Artigo
Язык:Inglês
Опубликовано: Springer Berlin Heidelberg 2020
Предметы:
Review
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC7429610/
https://ncbi.nlm.nih.gov/pubmed/32656747
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12551-020-00725-1
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