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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Vydáno v:Medicina (Kaunas)
Hlavní autoři: Abdallah, Atiyeh M, Carlus, S. Justin, Al-Mazroea, Abdulhadi H, Alluqmani, Mohammad, Almohammadi, Yousef, Bhuiyan, Zahurul A, Al-Harbi, Khalid M
Médium: Artigo
Jazyk:Inglês
Vydáno: MDPI 2019
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6359299/
https://ncbi.nlm.nih.gov/pubmed/30650640
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/medicina55010017
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