Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's disease
Year: 2020
Type: article
Study design: Observational Study
Source: Parkinsonism & Related Disorders
Language: English
Subfield: Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Funders: U.S. Department of Defense, Michael J. Fox Foundation for Parkinson's Research, Mayo Clinic, Mayo Foundation for Medical Education and Research, National Institutes of Health, Center for Individualized Medicine, Mayo Clinic, National Institute on Aging, National Institute of Mental Health, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke
Awards: Mitochondrial Sirtuin 3 in Parkinson's disease, Neuropsychiatric Disease-focused Exploration of Neuronal Regulatory Landscapes, Understanding the role of MAPT in Parkinsonian disorders, Predoctoral Training Program in Human Genetics, Development of a Neuronal Regulatory Lexicon, Molecular mechanisms of Parkin-directed mitochondrial quality control, Molecular mechanisms of PINK1-PRKN directed mitochondrial quality control, Identifying genes and Pathways that impact Tau Toxicity in FTD, Synergistic Interaction of amyloid-beta and alpha-synuclein in Lewy body Dementia, Genetics and Molecular Biology of Parkinsonism, Selective autophagy in Alzheimer's disease and related dementias
OpenAlex ID: W3046854691
