Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.

Hereditary dentatorubropallidoluysian atrophy (DRPLA) is an autosomal dominant neurodegenerative disorder. Clinical and genetic findings in hereditary DRPLA are very similar to those of Huntington's disease (HD). However, it can be differentiated from HD by the pathological findings of dentator...

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Detalhes bibliográficos
Publicado no:J Med Genet
Main Authors: Kondo, I, Ohta, H, Yazaki, M, Ikeda, J E, Gusella, J F, Kanazawa, I
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group 1990
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016930/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1969487/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.27.2.105
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