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Localization of the Gene for a Novel Autosomal Recessive Neurodegenerative Huntington-Like Disorder to 4p15.3

A consanguineous family affected by an autosomal recessive, progressive neurodegenerative Huntington-like disorder, was tested to rule out juvenile-onset Huntington disease (JHD). The disease manifests at ∼3–4 years and is characterized by both pyramidal and extrapyramidal abnormalities, including c...

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Auteurs principaux: Kambouris, M., Bohlega, S., Al-Tahan, A., Meyer , B. F.
Format: Artigo
Langue:Inglês
Publié: The American Society of Human Genetics 2000
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Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1288097/
https://ncbi.nlm.nih.gov/pubmed/10677304
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