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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 1, 2024. (Total: 233962Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Ataxia and PDYN[original query]
The frequency of spinocerebellar ataxia type 23 in a UK population.
Journal of neurology 2013 Mar 260 (3): 856-9.
Fawcett Katherine, Mehrabian Mohadeseh, Liu Yo-Tsen, Hamed Sherifa, Elahi Elahe, Revesz Tamas, Koutsis Georgios, Herscheson Joshua, Schottlaender Lucia, Wardle Mark, Morrison Patrick J, Morris Huw R, Giunti Paola, Wood Nicholas, Houlden Hen
Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia.
Movement disorders : official journal of the Movement Disorder Society 2012 Mar 27 (3): 442-6.
Fogel Brent L, Lee Ji Yong, Lane Jessica, Wahnich Amanda, Chan Sandy, Huang Alden, Osborn Greg E, Klein Eric, Mamah Catherine, Perlman Susan, Geschwind Daniel H, Coppola Giovan
Intrafamilial phenotypic variation in spinocerebellar ataxia type 23.
Cerebellum & ataxias 2020 6 7 7.
Satoh Shunichi, Kondo Yasufumi, Ohara Shinji, Yamaguchi Tomomi, Nakamura Katsuya, Yoshida Kunihi
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