Dystrophin Dp71 Subisoforms Localize to the Mitochondria of Human Cells
Dystrophin Dp71 Subisoforms Localize to the Mitochondria of Human Cells
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Basel: MDPI AG
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Language
English
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Basel: MDPI AG
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Duchenne muscular dystrophy (DMD) is a fatal muscle wasting disease caused by deficiency in dystrophin, a protein product encoded by the DMD gene. Mitochondrial dysfunction is now attracting much attention as a central player in DMD pathology. However, dystrophin has never been explored in human mitochondria. Here, we analyzed dystrophin in cDNAs a...
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Dystrophin Dp71 Subisoforms Localize to the Mitochondria of Human Cells
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TN_cdi_doaj_primary_oai_doaj_org_article_d3118a69f77543f59d055957917d2f72
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d3118a69f77543f59d055957917d2f72
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ISSN
2075-1729
E-ISSN
2075-1729
DOI
10.3390/life11090978
