Heterozygous Mylk3 Knockout Mice Partially Recapitulate Human DCM With Heterozygous MYLK3 Mutations

Backgrounds: Recent studies identified heterozygous variants in MYLK3 gene that encodes cardiac myosin light chain kinase (cMLCK) are related to familial dilated cardiomyopathy (DCM) for the first time. Autosomal dominant traits suggest that pathogenesis of DCM could be related to heterozygous MYLK3...

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Publicado en:Front Physiol
Autores principales: Tougas, Carson L., Grindrod, Tabor, Cai, Lawrence X., Alkassis, Fariz F., Kasahara, Hideko
Formato: Artigo
Lenguaje:Inglês
Publicado: Frontiers Media S.A. 2019
Materias:
Physiology
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6563786/
https://ncbi.nlm.nih.gov/pubmed/31244672
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2019.00696
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