Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype
Huntington's disease (HD) is a neurodegenerative disorder characterized by chorea, behavioral disturbances and dementia, caused by a pathological expansion of the CAG trinucleotide in the HTT gene. Several patients have been recognized with the typical HD phenotype without the expected mutation. The...
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| Päätekijät: | , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Thieme Revinter Publicações
2011-06-01
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| Sarja: | Arquivos de Neuro-Psiquiatria |
| Aiheet: | |
| Linkit: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2011000400002&lng=en&tlng=en |
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