Autosomal dominant Parkinson's disease caused by SNCA duplications-Reference-Cited by-同舟云学术

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Autosomal dominant Parkinson's disease caused by SNCA duplications

Published:2016-01 Issue: Volume:22 Page:S1-S6
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Konno Takuya,Ross Owen A.,Puschmann Andreas,Dickson Dennis W.,Wszolek Zbigniew K.

Funder

Uehara Memorial Foundation

NIH

Michael J. Fox Foundation

Mayo Clinic Center for Individualized Medicine

Mayo Clinic Neuroscience Focused Research Team

The Little Family Foundation

Swedish Parkinson Foundation

Swedish National Health Services

Bundy Academy, Sweden

Swedish Parkinson Academy

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference29 articles.

1. Genetics of Parkinson's disease: the yield;Spatola;Park. Relat. Disord.,2014

2. Monogenic Parkinson's disease and parkinsonism: clinical phenotypes and frequencies of known mutations;Puschmann;Park. Relat. Disord.,2013

3. A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants;Sharma;J. Med. Genet.,2012

4. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease;Polymeropoulos;Science,1997

5. Update on novel familial forms of Parkinson's disease and multiple system atrophy;Fujioka;Park. Relat. Disord.,2014

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