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Journal of Human Genetics|September 14, 2019
UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomesHaitian Nan, Yuta Ichinose, Masaki Tanaka, et al.Parkinsonism & Related Disorders|December 12, 2018
Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletionYuta Ichinose, Hiroyuki Ishiura, Masaki Tanaka, et al.Brain : a Journal of Neurology|March 24, 2020
Variants in saposin D domain of prosaposin gene linked to Parkinson's diseaseYutaka Oji, Taku Hatano, Shin-Ichi Ueno, et al.Neurobiology of Aging|July 28, 2020
The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1Arisa Hayashida, Yuanzhe Li, Hiroyo Yoshino, et al.Pageof 3