TY - JOUR T1 - 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 JF - Journal of Human Genetics Y1 - 2006 A1 - Costa, M.D.C. A1 - Teixeira-Castro, A. A1 - Constante, M. A1 - Magalhães, M. A1 - Magalhães, P. A1 - Cerqueira, J. A1 - Vale, J. A1 - Passão, V. A1 - Barbosa, C. A1 - Robalo, C. A1 - Coutinho, P. A1 - Barros, J. A1 - Santos, M.M. A1 - Sequeiros, J. A1 - MacIel, P. VL - 51 UR - http://www.scopus.com/inward/record.url?eid=2-s2.0-77952878970&partnerID=40&md5=06556bbe8033f2aee296c9362b5a1d3a IS - 8 N1 - Cited By (since 1996): 13Export Date: 18 March 2013Source: Scopus ER - TY - JOUR T1 - Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement JF - Neurology Y1 - 2005 A1 - MacIel, P. A1 - Cruz, V.T. A1 - Constante, M. A1 - Iniesta, I. A1 - Costa, M.C. A1 - Gallati, S. A1 - Sousa, N. A1 - Sequeiros, J. A1 - Coutinho, P. A1 - Santos, M.M. VL - 65 UR - http://www.scopus.com/inward/record.url?eid=2-s2.0-23844553465&partnerID=40&md5=bb8e13589c21c86197ce6d8411a2f0a8 IS - 4 N1 - Cited By (since 1996): 34Export Date: 18 March 2013Source: Scopus ER -