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Late-onset Huntington’s disease with 40–42 CAG expansion
INTRODUCTION: Huntington’s disease (HD) is a rare autosomal dominant neurodegenerative disorder caused by a CAG expansion greater than 35 in the IT-15 gene. There is an inverse correlation between the number of pathological CAG and the age of onset. However, CAG repeats between 40 and 42 showed a wi...
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| Publicado no: | Neurol Sci |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer International Publishing
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7160095/ https://ncbi.nlm.nih.gov/pubmed/31820322 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10072-019-04177-8 |
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