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About this Biochemistry, Genetics and Molecular Biology article
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 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 is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- 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
- Publisher
- Nature Publishing Group; Springer Science and Business Media LLC; Springer Verlag (ISSN 1435-232X)
- Published
- 2006
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)