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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Veröffentlicht in:Iran J Public Health
Hauptverfasser: SAGHAFI, Hoorieh, HAGHJOO, Majid, SABBAGH, Sima, SAMIEE, Niloofar, VAKILIAN, Farve, SALEHI OMRAN, Mohammad Taghi, DADASHI, Masoomeh, AMIN, Ahmad, KERAMATIPOUR, Mohammad
Format: Artigo
Sprache:Inglês
Veröffentlicht: Tehran University of Medical Sciences 2016
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Original Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4851747/
https://ncbi.nlm.nih.gov/pubmed/27141495
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