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

Title	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
Publication Type	Journal Article
Year of Publication	2006
Authors	Costa, MDC, Teixeira-Castro, A, Constante, M, Magalhães, M, Magalhães, P, Cerqueira, J, Vale, J, Passão, V, Barbosa, C, Robalo, C, Coutinho, P, Barros, J, Santos, MM, Sequeiros, J, MacIel, P
Journal	Journal of Human Genetics
Volume	51
Issue	8
Pagination	645 - 651
Date Published	2006///
URL	http://www.scopus.com/inward/record.url?eid=2-s2.0-77952878970&partnerID=40&md5=06556bbe8033f2aee296c9362b5a1d3a

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