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Paper Details

Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 loci.
Brain
24
2022
16q11, KANSL1, KAT8, MAPT, MAPT H1 loci, MAPT gene, NSL complex, PINK1, Parkinson's disease, chromosome 17q21, familial Parkinson's disease, idiopathic Parkinson's disease, lysine, neurodegeneration, neurodegenerative disease, risk genes, risk loci
Author NameAffiliation
Henry HouldenUCL Queen Square Institute of Neurology
Nicholas W Wood
Nicholas W WoodUCL Queen Square Institute of Neurology
Nicholas W Wood
Nicholas W WoodUCL Queen Square Institute of Neurology
Andrew B SingletonNational Institute on Aging, National Institutes of Health
Andrew B SingletonCenter for Alzheimer's and Related Dementias, National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health
Andrew B SingletonNational Institute on Aging, National Institutes of Health
Andrew B SingletonCenter for Alzheimer's and Related Dementias, National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health
Mina Ryten
Mina RytenNIHR Great Ormond Street Hospital Biomedical Research Centre, University College London
Mina RytenGreat Ormond Street Institute of Child Health, University College London
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Release 1.2