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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 9, 2024. (Total: 232364Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Spinocerebellar Ataxias and PDYN[original query]
Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.
American journal of human genetics 2011 Jul 89 (1): 121-30.
Kobayashi Hatasu, Abe Koji, Matsuura Tohru, Ikeda Yoshio, Hitomi Toshiaki, Akechi Yuji, Habu Toshiyuki, Liu Wanyang, Okuda Hiroko, Koizumi Ak
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
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