Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Ataxia and SCA13[original query] |
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Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13). PloS one 2011 6 (3): e17811. Figueroa Karla P, Waters Michael F, Garibyan Vartan, Bird Thomas D, Gomez Christopher M, Ranum Laura P W, Minassian Natali A, Papazian Diane M, Pulst Stefan |
Spinocerebellar ataxia type 13 is an uncommon SCA subtype in the Chinese Han population. The International journal of neuroscience 2013 Jan . Peng L, Wang C, Chen Z, Wang JL, Tang BS, Jiang H |
Functional analysis helps to define KCNC3 mutational spectrum in Dutch ataxia cases. PloS one 2015 10 (3): e0116599. Duarri Anna, Nibbeling Esther A R, Fokkens Michiel R, Meijer Michel, Boerrigter Melissa, Verschuuren-Bemelmans Corien C, Kremer Berry P H, van de Warrenburg Bart P, Dooijes Dennis, Boddeke Erik, Sinke Richard J, Verbeek Dineke |
V374A KCND3 Pathogenic Variant Associated With Paroxysmal Ataxia Exacerbations. Neurology. Genetics 2021 Feb 7 (1): e546. Paucar Martin, Ågren Richard, Li Tianyi, Lissmats Simon, Bergendal Åsa, Weinberg Jan, Nilsson Daniel, Savichetva Irina, Sahlholm Kristoffer, Nilsson Johanna, Svenningsson P |
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