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Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.

OBJECTIVE--To investigate the molecular genetic basis of the cause of disease in a family with hypertrophic cardiomyopathy. BACKGROUND--Mutation within the beta cardiac myosin heavy chain gene has been shown to be the pathogenetic mechanism underlying the disease in several families, though clear ev...

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Hlavní autoři: al-Mahdawi, S, Chamberlain, S, Cleland, J, Nihoyannopoulos, P, Gilligan, D, French, J, Choudhury, L, Williamson, R, Oakley, C
Médium: Artigo
Jazyk:Inglês
Vydáno: 1993
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1024940/
https://ncbi.nlm.nih.gov/pubmed/8435239
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