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Paper Details

Huntington's Disease Pathogenesis: Two Sequential Components.
Journal of Huntington's disease
30
2021
DNA polymorphisms, HD, HTT, HTT locus, Human, Human Genome, Huntington's Disease, Huntington's disease, OMIM #, autosomal disease, chromosome 4p16, cognitive decline, familial neurodegenerative disorder, genetic defect, human, human chromosomes, psychiatric disturbances
Author NameAffiliation
Marcy E MacDonaldCenter for Genomic Medicine, Massachusetts General Hospital
Marcy E MacDonaldHarvard Medical School
Marcy E MacDonaldthe Broad Institute of M.I.T. and Harvard
Peter HolmansMedical Research Council (MRC) Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurology, Cardiff University
James F GusellaCenter for Genomic Medicine, Massachusetts General Hospital
James F Gusellathe Broad Institute of M.I.T. and Harvard
James F GusellaBlavatnik Institute, Harvard Medical School
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