Early-onset Parkinson's disease due to PINK1 p.Q456X mutation – Clinical and functional study-Reference-Cited by-同舟云学术

Early-onset Parkinson's disease due to PINK1 p.Q456X mutation – Clinical and functional study

Published:2014-11 Issue:11 Volume:20 Page:1274-1278
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Siuda Joanna,Jasinska-Myga Barbara,Boczarska-Jedynak Magdalena,Opala Grzegorz,Fiesel Fabienne C.,Moussaud-Lamodière Elisabeth L.,Scarffe Leslie A.,Dawson Valina L.,Ross Owen A.,Springer Wolfdieter,Dawson Ted M.,Wszolek Zbigniew K.

Funder

NIH

Mayo Clinic Center

GHR Foundation

Marriott Family Foundation

Gerstner Family Career Development Award

JPB Foundation

Adrienne Helis Malvin Medical Research Foundation

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference12 articles.

1. Early-onset parkinsonism associated with PINK1 mutations. Frequency, genotypes and phenotypes;Bonifati;Neurology,2005

2. Homozygous and heterozygous PINK1 mutations: considerations for diagnosis and care of Parkinson's disease patients;Zadikoff;Mov Disord,2006

3. Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa;Ibanez;Brain,2006

4. Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease;Hedrich;Arch Neurol,2006

5. PINK1 mutations and parkinsonism;Ishihara-Paul;Neurology,2008

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