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miR-381 Attenuates Peripheral Neuropathic Phenotype Caused by Overexpression of PMP22
Charcot-Marie Tooth disease type 1A (CMT1A), the major type of CMT, is caused by duplication of peripheral myelin protein 22 (PMP22) gene whose overexpression causes structural and functional abnormalities in myelination. We investigated whether miRNA-mediated regulation of PMP22 expression could re...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Brain and Neural Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6526106/ https://www.ncbi.nlm.nih.gov/pubmed/31138995 http://dx.doi.org/10.5607/en.2019.28.2.279 |