Comprehensive assessment of PINK1 variants in Parkinson's disease-Reference-Cited by-同舟云学术

Comprehensive assessment of PINK1 variants in Parkinson's disease

Published:2020-07 Issue: Volume:91 Page:168.e1-168.e5
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Krohn Lynne^ORCID,Grenn Francis P.,Makarious Mary B.,Kim Jonggeol Jeffrey,Bandres-Ciga Sara^ORCID,Roosen Dorien A.,Gan-Or Ziv^ORCID,Nalls Mike A.,Singleton Andrew B.,Blauwendraat Cornelis

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference29 articles.

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2. “Parkinson’s disease age at onset genome-wide association study: defining heritability, genetic Loci, and α-synuclein mechanisms.”;Blauwendraat;Mov. Disord.,2019

3. “Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson’s disease;Blauwendraat;Neurobiol. Aging,2018

4. “The genetic architecture of Parkinson’s disease;Blauwendraat;Lancet Neurol.,2019

5. Frequency of loss of function variants in LRRK2 in Parkinson disease;Blauwendraat;JAMA Neurol.,2018

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