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Association of UBQLN1 mutation with Brown-Vialetto-Van Laere syndrome but not typical ALS
Genetic variants in UBQLN1 gene have been linked to neurodegeneration and mutations in UBQLN2 have recently been identified as a rare cause of amyotrophic lateral sclerosis (ALS). OBJECTIVE: To test if genetic variants in UBQLN1 are involved in ALS. METHODS: 102 and 94 unrelated patients with famili...
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| Опубликовано в: : | Neurobiol Dis |
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| Главные авторы: | , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2012
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4245016/ https://ncbi.nlm.nih.gov/pubmed/22766032 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2012.06.018 |
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