Dystrophin Dp71 Subisoforms Localize to the Mitochondria of Human Cells

Duchenne muscular dystrophy (DMD) is a fatal muscle wasting disease caused by deficiency in dystrophin, a protein product encoded by the <i>DMD</i> gene. Mitochondrial dysfunction is now attracting much attention as a central player in DMD pathology. However, dystrophin has never been ex...

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Bibliographic Details
Main Authors: Emma Tabe Eko Niba, Hiroyuki Awano, Tomoko Lee, Yasuhiro Takeshima, Masakazu Shinohara, Hisahide Nishio, Masafumi Matsuo
Format: Article
Language:English
Published: MDPI AG 2021-09-01
Series:Life
Subjects:
Online Access:https://www.mdpi.com/2075-1729/11/9/978