Identification of DAPK1 as an autophagy-related biomarker for myotonic dystrophy type 1
Myotonic dystrophy type I (DM1), a CTG repeat expansion hereditary disorder, is primarily characterized by myotonia. Several studies have reported that abnormal autophagy pathway has a close relationship with DM1. However, the underlying key regulatory molecules dictating autophagy disturbance still...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
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Frontiers Media S.A.
2022-10-01
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| Edice: | Frontiers in Genetics |
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| On-line přístup: | https://www.frontiersin.org/articles/10.3389/fgene.2022.1022640/full |
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