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Correlation of clinical and molecular features in spinal bulbar muscular atrophy
OBJECTIVES: To characterize the clinical and genetic features of spinal bulbar muscular atrophy (SBMA), a rare neurodegenerative disorder caused by the expansion of a CAG repeat in the first exon of the androgen receptor gene, in the United Kingdom. METHODS: We created a national register for SBMA i...
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| Autors principals: | , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Lippincott Williams & Wilkins
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4075620/ https://ncbi.nlm.nih.gov/pubmed/24814851 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000000507 |
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