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Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease.

Authors :
Lesage S
Bras J
Cormier-Dequaire F
Condroyer C
Nicolas A
Darwent L
Guerreiro R
Majounie E
Federoff M
Heutink P
Wood NW
Gasser T
Hardy J
Tison F
Singleton A
Brice A
Source :
Neurology. Genetics [Neurol Genet] 2015 Jun 18; Vol. 1 (1), pp. e9. Date of Electronic Publication: 2015 Jun 18 (Print Publication: 2015).
Publication Year :
2015

Abstract

Rab proteins are small molecular weight guanosine triphosphatases involved in the regulation of vesicular trafficking.(1) Three of 4 X-linked RAB genes are specific to the brain, including RAB39B. Recently, Wilson et al.(2) reported that mutations in RAB39B cause X-linked intellectual disability (ID) and pathologically confirmed Parkinson disease (PD). They identified a ∼45-kb deletion resulting in the complete loss of RAB39B in an Australian kindred and a missense mutation in a large Wisconsin kindred. Here, we report an additional affected man with typical PD and mild mental retardation harboring a new truncating mutation in RAB39B.

Details

Language :
English
ISSN :
2376-7839
Volume :
1
Issue :
1
Database :
MEDLINE
Journal :
Neurology. Genetics
Publication Type :
Academic Journal
Accession number :
27066548
Full Text :
https://doi.org/10.1212/NXG.0000000000000009