Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy

Background and objectives: Dilated cardiomyopathy (DCM) is a rare cardiac disease characterised by left ventricular enlargement, reduced left ventricular contractility, and impaired systolic function. Childhood DCM is clinically and genetically heterogenous and associated with mutations in over 100...

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Xehetasun bibliografikoak
Egile Nagusiak: Atiyeh M Abdallah, S. Justin Carlus, Abdulhadi H Al-Mazroea, Mohammad Alluqmani, Yousef Almohammadi, Zahurul A Bhuiyan, Khalid M Al-Harbi
Formatua: Artikulua
Hizkuntza:English
Argitaratua: MDPI AG 2019-01-01
Saila:Medicina
Gaiak:
Sarrera elektronikoa:http://www.mdpi.com/1010-660X/55/1/17