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Genetic variations of α-cardiac actin and cardiac muscle LIM protein in hypertrophic cardiomyopathy in South India

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is a disease of the heart muscle, with an autosomal dominant mode of inheritance. It is also known as the ‘disease of the sarcomere’, and is a major cause of morbidity and mortality worldwide. Mutations in the sarcomeric genes have been largely implicate...

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Detalhes bibliográficos
Main Authors: Rangaraju, Advithi, Rani, Deepa Selvi, Satyanarayana, ML, Calambur, Narasimhan, Swapna, Nalla, Nallari, Pratibha
Formato: Artigo
Idioma:Inglês
Publicado em: Pulsus Group Inc 2012
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3383364/
https://ncbi.nlm.nih.gov/pubmed/23204897
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