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Molecular pathogenesis of spinal bulbar muscular atrophy (Kennedy’s disease) and avenues for treatment
PURPOSE OF REVIEW: To illustrate the current understanding and avenues for developing treatment in spinal and bulbar muscular atrophy (SBMA), an inherited neuromuscular disorder caused by a CAG trinucleotide repeat expansion in the androgen receptor (AR) gene. RECENT FINDINGS: Important advances hav...
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| Publicat a: | Curr Opin Neurol |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7748295/ https://ncbi.nlm.nih.gov/pubmed/32773451 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WCO.0000000000000856 |
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