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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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Xehetasun bibliografikoak
Argitaratua izan da:J Med Genet
Egile Nagusiak: Kondo, I, Ohta, H, Yazaki, M, Ikeda, J E, Gusella, J F, Kanazawa, I
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BMJ Publishing Group 1990
Gaiak:
Sarrera elektronikoa: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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