Human Genome Epidemiology Literature Finder
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Query Trace: Cerebellar Ataxia and PLEKHG4[original query] |
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Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population. Journal of human genetics 2006 51 (4): 363-7. Wieczorek Stefan, Arning Larissa, Alheite Ingrid, Epplen Jörg |
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- Page last updated:Jun 02, 2023
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