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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Bibliographic Details
Published in:	J Med Genet
Main Authors:	Kondo, I, Ohta, H, Yazaki, M, Ikeda, J E, Gusella, J F, Kanazawa, I
Format:	Artigo
Language:	Inglês
Published:	BMJ Publishing Group 1990
Subjects:	Research Article
Online Access:	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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Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.

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