Mutations in DJ-1 are rare in familial Parkinson disease

Mutations in DJ-1 (PARK7) are one cause of early-onset autosomal-recessive parkinsonism. We screened for DJ-1 mutations in 93 affected individuals from the 64 multiplex Parkinson disease (PD) families in our sample that had the highest family-specific multipoint LOD scores at the DJ-1 locus. In addi...

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主要な著者: Pankratz, Nathan, Pauciulo, Michael W., Elsaesser, Veronika E., Marek, Diane K., Halter, Cheryl A., Wojcieszek, Joanne, Rudolph, Alice, Shults, Clifford W., Foroud, Tatiana, Nichols Ph.D., William C.
フォーマット: Artigo
言語:Inglês
出版事項: 2006
主題:
Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1706076/
https://ncbi.nlm.nih.gov/pubmed/16997464
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2006.09.003
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