Cardiac and Skeletal Muscle Defects in a Mouse Model of Human Barth Syndrome

Barth syndrome is an X-linked genetic disorder caused by mutations in the tafazzin (taz) gene and characterized by dilated cardiomyopathy, exercise intolerance, chronic fatigue, delayed growth, and neutropenia. Tafazzin is a mitochondrial transacylase required for cardiolipin remodeling. Although ta...

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Detalhes bibliográficos
Main Authors: Acehan, Devrim, Vaz, Frederic, Houtkooper, Riekelt H., James, Jeanne, Moore, Vicky, Tokunaga, Chonan, Kulik, Willem, Wansapura, Janaka, Toth, Matthew J., Strauss, Arnold, Khuchua, Zaza
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2011
Assuntos:
Bioenergetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3020775/
https://ncbi.nlm.nih.gov/pubmed/21068380
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M110.171439
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