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Direct relationship between increased expression and mistrafficking of the Charcot–Marie–Tooth–associated protein PMP22
Charcot–Marie–Tooth disease (CMT) is a neuropathy of the peripheral nervous system that afflicts ∼1:2500 people. The most common form of this disease (CMT1A, 1:4000) is associated with duplication of chromosome fragment 17p11.2-12, which results in a third WT PMP22 allele. In rodent models overexpre...
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| Publicat a: | J Biol Chem |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Biochemistry and Molecular Biology
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7443497/ https://ncbi.nlm.nih.gov/pubmed/32647009 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.AC120.014940 |
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