Related Experiment Video
Updated: Aug 30, 2026

High Content Screening in Neurodegenerative Diseases
Published on: January 6, 2012
Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism
P Ibáñez1, G De Michele, V Bonifati
1INSERM U289, Neurologie et Thérapeutique Expérimentale, Hôpital de la Pitié-Salpêtrière, Paris, France.
Abstract:
The DJ-1 gene was identified as responsible for early onset autosomal recessive parkinsonism in two families (PARK7). In this study, after excluding mutations in the parkin gene, the authors screened a large series of early onset autosomal recessive parkinsonism families and consanguineous isolated patients of diverse geographic origins for DJ-1 mutations. No mutations were found. This indicates that PARK7 is not a common locus for early onset autosomal recessive parkinsonism, and that one or more new loci remains to be identified.
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