MAPT haplotype diversity in multiple system atrophy
Year: 2016
Type: article
Study design: Observational Study
Source: Parkinsonism & Related Disorders
Authors: Catherine Labbé, Michael G. Heckman, Oswaldo Lorenzo-Betancor, Melissa E. Murray, Kotaro Ogaki, Alexandra I. Soto-Ortolaza, Ronald L. Walton, Shinsuke Fujioka, Shunsuke Koga, Ryan J. Uitti, Jay A. van Gerpen, Ronald C. Petersen, Neill R. Graff-Radford, Steven G. Younkin, Bradley F. Boeve, William P. Cheshire, Phillip A. Low, Paola Sandroni, Elizabeth A. Coon, Wolfgang Singer, Zbigniew K. Wszolek, Dennis W. Dickson, Owen A. Ross
Institutions: Mayo Clinic, Mayo Clinic in Florida
Language: English
Subfield: Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funders: Michael J. Fox Foundation for Parkinson's Research, Mayo Clinic, National Institutes of Health, U.S. Food and Drug Administration, Center for Individualized Medicine, Mayo Clinic, Tau Consortium, National Institute on Aging, National Institute of Neurological Disorders and Stroke, National Center for Research Resources
Awards: Pathogenesis and Diagnosis of Multiple System Atrophy (P01), G2212362641, Understanding the role of MAPT in Parkinsonian disorders, G3308772956, Alzheimers Disease Patient Registry, G413369726, Autonomic Rare Diseases Clinical Research Consortium, Genetics and Molecular Biology of Parkinsonism, Differential Approach to the Postural Tachycardia Syndrome, Mayo Clinic Center for Translational Science Activities, Synucleinopathies – Novel Targets in Early Diagnosis, Pathophysiology, and Therapeutic Approach, Mayo Alzheimer's Disease Research Center
OpenAlex ID: W2440804174