Role of <i>Tafazzin</i> in Mitochondrial Function, Development and Disease
<i>Tafazzin</i>, 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 w...
Gorde:
| Egile Nagusiak: | , |
|---|---|
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
MDPI AG
2020-05-01
|
| Saila: | Journal of Developmental Biology |
| Gaiak: | |
| Sarrera elektronikoa: | https://www.mdpi.com/2221-3759/8/2/10 |
| Etiketak: |
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!
|