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Filters: Author is Alcaraz, Wendy  [Clear All Filters]
2018
Noch E, Henchcliffe C, Hellmers N, Chu MLynn, Pappas J, Moran E, Alcaraz W, Sarva H.  2018.  Kufor-Rakeb Syndrome Due to a Novel ATP13A2 Mutation in 2 Chinese-American Brothers.. Mov Disord Clin Pract. 5(1):92-95.