Human Genome Epidemiology Literature Finder
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Query Trace: Alzheimer Disease and NOP56[original query] |
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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 |
- Page last reviewed:Feb 1, 2024
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