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 - Costa, M.D.C.; Teixeira-Castro, A.; Constante, M.; Magalhães, M.; Magalhães, P.; Cerqueira, J.; Vale, J.; Passão, V.; Barbosa, C.; Robalo, C.; Coutinho, P.; Barros, J.; et al. (Journal of Human Genetics, 2006)
Cited By (since 1996): 13Export Date: 18 March 2013Source: Scopus