Barth syndrome mutations that cause tafazzin complex lability

Deficits in mitochondrial function result in many human diseases. The X-linked disease Barth syndrome (BTHS) is caused by mutations in the tafazzin gene TAZ1. Its product, Taz1p, participates in the metabolism of cardiolipin, the signature phospholipid of mitochondria. In this paper, a yeast BTHS mu...

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Detalles Bibliográficos
Autores principales: Claypool, Steven M., Whited, Kevin, Srijumnong, Santi, Han, Xianlin, Koehler, Carla M.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2011
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101092/
https://www.ncbi.nlm.nih.gov/pubmed/21300850
http://dx.doi.org/10.1083/jcb.201008177

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101092/
https://www.ncbi.nlm.nih.gov/pubmed/21300850
http://dx.doi.org/10.1083/jcb.201008177

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