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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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Bibliographische Detailangaben
Hauptverfasser:	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.
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	2006
Schlagworte:	Article
Online Zugang:	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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Mutations in DJ-1 are rare in familial Parkinson disease

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