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Homozygous deletion mutation of the parkin gene in patients with atypical parkinsonism

Autosomal recessive juvenile parkinsonism (AR-JP) is characterised by homogenous clinical features and selective degeneration of nigral neurons. Recent progress in molecular genetic analyses of AR-JP has led to the identification of a novel ubiquitin-like protein, parkin, whose precise function stil...

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書誌詳細
主要な著者: Kuroda, Y, Mitsui, T, Akaike, M, Azuma, H, Matsumoto, T
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Group 2001
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1737499/
https://ncbi.nlm.nih.gov/pubmed/11459900
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.71.2.231
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