Role of Tafazzin in Mitochondrial Function, Development and Disease

Tafazzin, an enzyme associated with the rare inherited x-linked disorder Barth Syndrome, is a nuclear encoded mitochondrial transacylase that is highly conserved across multiple species and plays an important role in mitochondrial function. Numerous studies have elucidated the mechanisms by which Ta...

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Detalles Bibliográficos
Autores principales: Chin, Michael T., Conway, Simon J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344621/
https://www.ncbi.nlm.nih.gov/pubmed/32456129
http://dx.doi.org/10.3390/jdb8020010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344621/
https://www.ncbi.nlm.nih.gov/pubmed/32456129
http://dx.doi.org/10.3390/jdb8020010

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