1 document found, page 1 of 1

Sort by Issue Date

Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL gen...

Costa, Maria do Carmo; Teixeira-Castro, Andreia; Constante, Marco; Magalhães, Marina; Magalhães, Paula; Cerqueira, Joana; Vale, José; Passão, Vitorina

Huntington disease (HD) is an autosomal dominant neurodegenerative disorder characterised by chorea, cognitive impairment, dementia and personality changes, caused by the expansion of a CAG repeat in the HD gene. Often, patients with a similar clinical presentation do not carry expansions of the CAG repeat in this gene [Huntington disease-like (HDL) patients]. We report the genetic analysis of 107 Portuguese pa...


1 Results

Queried text

Refine Results

Author
















More optionsLess options

Date


Document Type


Access rights


Resource


Subject





















More optionsLess options