A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family-Reference-Cited by-同舟云学术

A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family

Published:2016-08 Issue: Volume:29 Page:117-120
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Hanagasi Hasmet A.,Giri Anamika,Kartal Ece,Guven Gamze,Bilgiç Başar,Hauser Ann-Kathrin,Emre Murat,Heutink Peter,Basak Nazlı,Gasser Thomas,Simón-Sánchez Javier,Lohmann Ebba

Funder

Boğaziçi University

Inan Kıraç Foundation

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference16 articles.

1. Mutations in the DJ1 gene associated with autosomal recessive early-onset parkinsonism;Bonifati;Science,2003

2. Analysis of an early-onset Parkinson's disease cohort for DJ1 mutations;Clark;Mov. Disord.,2004

3. Mutation analysis of Parkin, PINK1, DJ1 and ATP13A2 genesin Chinese patients with autosomal recessive early-onset parkinsonism;Guo;Mov. Disord.,2008

4. Parkinson study group – PRO-GENI investigators. Mutations in DJ1 are rare in familial Parkinson disease;Pankratz;Neurosci. Lett.,2006

5. Atypical parkinsonism-dystonia syndrome caused by a novel DJ1 mutation;Bras;Mov. Disord. Clin. Pract.,2014

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