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DNAJB6 Myopathies: Focused Review on an Emerging and Expanding Group of Myopathies
Mutations in the DNAJB6 gene have been associated with the autosomal dominant limb girdle muscular dystrophy type 1D (LGMD1D), a disorder characterized by abnormal protein aggregates and rimmed vacuoles in muscle fibers. DNAJB6 is a ubiquitously expressed Hsp40 co-chaperone characterized by a J doma...
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| Опубликовано в: : | Front Mol Biosci |
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| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Frontiers Media S.A.
2016
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5043021/ https://ncbi.nlm.nih.gov/pubmed/27747217 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fmolb.2016.00063 |
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