Setting up Multiplex Panels for Genetic Testing of Familial Hypertrophic Cardiomyopathy Based on Linkage Analysis

BACKGROUND: Familial hypertrophic cardiomyopathy (HCM) is caused by mutations in genes encoding cardiac sarcomere proteins. Nowadays genetic testing of HCM plays an important role in clinical practice by contributing to the diagnosis, prognosis, and screening of high-risk individuals. The aim of thi...

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Detalles Bibliográficos
Autores principales: SAGHAFI, Hoorieh, HAGHJOO, Majid, SABBAGH, Sima, SAMIEE, Niloofar, VAKILIAN, Farve, SALEHI OMRAN, Mohammad Taghi, DADASHI, Masoomeh, AMIN, Ahmad, KERAMATIPOUR, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4851747/
https://www.ncbi.nlm.nih.gov/pubmed/27141495

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4851747/
https://www.ncbi.nlm.nih.gov/pubmed/27141495

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