A new gene for Parkinson's disease: should we care?
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology
Reference8 articles.
1. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study;Funayama;Lancet Neurol,2015
2. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease;Nalls;Nat Genet,2014
3. Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders;Novarino;Science,2014
4. Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease;Beilina;Proc Natl Acad Sci USA,2014
5. RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease risk;Macleod;Neuron,2013
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1. What have we learned from genome-wide association studies (GWAS) in Parkinson's disease?;Ageing Research Reviews;2022-08
2. Progress toward an integrated understanding of Parkinson’s disease;F1000Research;2017-07-12
3. Orphan proteins of unknown function in the mitochondrial intermembrane space proteome: New pathways and metabolic cross-talk;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2016-11
4. Mutational scanning of the CHCHD2 gene in Han Chinese patients with Parkinson’s disease and meta-analysis of the literature;Parkinsonism & Related Disorders;2016-08
5. CHCHD2 and Parkinson's disease;The Lancet Neurology;2015-07
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