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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Detalles Bibliográficos
Autores principales: Abdallah, Atiyeh M, Carlus, S. Justin, Al-Mazroea, Abdulhadi H, Alluqmani, Mohammad, Almohammadi, Yousef, Bhuiyan, Zahurul A, Al-Harbi, Khalid M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359299/
https://www.ncbi.nlm.nih.gov/pubmed/30650640
http://dx.doi.org/10.3390/medicina55010017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359299/
https://www.ncbi.nlm.nih.gov/pubmed/30650640
http://dx.doi.org/10.3390/medicina55010017

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