Barth Syndrome Cardiomyopathy: An Update

Barth syndrome (BTHS) is an X-linked mitochondrial lipid disorder caused by mutations in the TAFAZZIN (TAZ) gene, which encodes a mitochondrial acyltransferase/transacylase required for cardiolipin (CL) biosynthesis. Cardiomyopathy is a major clinical feature of BTHS. During the past four decades, w...

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Detalles Bibliográficos
Autores principales: Pang, Jing, Bao, Yutong, Mitchell-Silbaugh, Kalia, Veevers, Jennifer, Fang, Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030331/
https://www.ncbi.nlm.nih.gov/pubmed/35456462
http://dx.doi.org/10.3390/genes13040656

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030331/
https://www.ncbi.nlm.nih.gov/pubmed/35456462
http://dx.doi.org/10.3390/genes13040656

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