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Exclusion of mutations in thePRNP,JPH3,TBP,ATN1,CREBBP,POU3F2andFTLgenes as a cause of disease in Portuguese patients with a Huntington-like phenotype

✍ Scribed by Maria do Carmo Costa; Andreia Teixeira-Castro; Marco Constante; Marina Magalhães; Paula Magalhães; Joana Cerqueira; José Vale; Vitorina Passão; Célia Barbosa; Conceição Robalo; Paula Coutinho; José Barros; Manuela M. Santos; Jorge Sequeiros; Patrícia Maciel


Book ID
106251994
Publisher
Nature Publishing Group
Year
2006
Tongue
English
Weight
176 KB
Volume
51
Category
Article
ISSN
1435-232X

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