Article
Creutzfeldt-Jakob disease with PRNP G114V mutation in a Chinese family.
Acta neurologica Scandinavica - 1 Jun 2010
Liu Z, Jia L, Piao Y, Lu D, Wang F, Lv H, Lu Y, Jia J
Abstract excerpt
BACKGROUND: Recent evidence has shown clinical phenotypic heterogeneity of inherited prion diseases, even between patients harbouring the same mutation in the PRNP gene. OBJECTIVE AND METHODS: We collected clinical data from a Chinese family with autosomal dominant dementia and screened the PRNP...
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