Human Genome Epidemiology Literature Finder
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Query Trace: Chorea and TBP[original query] |
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Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype. Journal of human genetics 2006 51 (8): 645-51. Costa Maria do Carmo, Teixeira-Castro Andreia, Constante Marco, Magalhães Marina, Magalhães Paula, Cerqueira Joana, Vale José, Passão Vitorina, Barbosa Célia, Robalo Conceição, Coutinho Paula, Barros José, Santos Manuela M, Sequeiros Jorge, Maciel Patríc |
Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study. BMC neurology 2015 15 (1): 166. Choubtum Lulin, Witoonpanich Pirada, Hanchaiphiboolkul Suchat, Bhidayasiri Roongroj, Jitkritsadakul Onanong, Pongpakdee Sunsanee, Wetchaphanphesat Suppachok, Boonkongchuen Pairoj, Pulkes Teerato |
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