%0 Journal Article %J Journal of Human Genetics %D 2006 %T 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 %A Costa, M.D.C. %A Teixeira-Castro, A. %A Constante, M. %A Magalhães, M. %A Magalhães, P. %A Cerqueira, J. %A Vale, J. %A Passão, V. %A Barbosa, C. %A Robalo, C. %A Coutinho, P. %A Barros, J. %A Santos, M.M. %A Sequeiros, J. %A MacIel, P. %B Journal of Human Genetics %V 51 %P 645 - 651 %8 2006/// %G eng %U http://www.scopus.com/inward/record.url?eid=2-s2.0-77952878970&partnerID=40&md5=06556bbe8033f2aee296c9362b5a1d3a %N 8 %0 Journal Article %J Neurology %D 2005 %T Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement %A MacIel, P. %A Cruz, V.T. %A Constante, M. %A Iniesta, I. %A Costa, M.C. %A Gallati, S. %A Sousa, N. %A Sequeiros, J. %A Coutinho, P. %A Santos, M.M. %B Neurology %V 65 %P 603 - 605 %8 2005/// %G eng %U http://www.scopus.com/inward/record.url?eid=2-s2.0-23844553465&partnerID=40&md5=bb8e13589c21c86197ce6d8411a2f0a8 %N 4