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A Case of Juvenile Huntington Disease in a 6-Year-Old Boy
Huntington disease is a neurodegenerative disorder distinguished by the triad of dominant inheritance, choreoathetosis and dementia, usually with onset in the fourth and fifth decades. It is caused by an unstable cytosine-adenine-guanine (CAG) trinucleotide repeat expansion in the gene IT15 in locus...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Korean Movement Disorder Society
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4027671/ https://ncbi.nlm.nih.gov/pubmed/24868381 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14802/jmd.10012 |
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