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pro vyhledávání: '"Elijah K Quinones"'
Autor:
Sandeep Kumar Barodia, Elijah K Quinones, Rita M. Cowell, Laura J. McMeekin, Rose B. Creed, Matthew S. Goldberg
Publikováno v:
NPJ Parkinson's Disease
npj Parkinson's Disease, Vol 5, Iss 1, Pp 1-9 (2019)
npj Parkinson's Disease, Vol 5, Iss 1, Pp 1-9 (2019)
Loss-of-function mutations in PINK1 are causally linked to recessively inherited Parkinson’s disease (PD), with marked loss of dopaminergic neurons in the substantia nigra that are required for normal movement. PINK1 is a nuclear-encoded mitochondr