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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

AuthID
P-004-J6S

Author(s)

Costa, MD

Teixeira Castro, A

Constante, M

Magalhaes, M

Magalhaes, P

Cerqueira, J

Vale, J

Passao, V

Barbosa, C

Robalo, C

Tipo de Documento

Article

Year published

2006

Publicado

in JOURNAL OF HUMAN GENETICS, ISSN: 1434-5161

Volume: 51, Número: 8, Páginas: 645-651 (7)

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Publication Identifiers

DOI: 10.1007/s10038-006-0001-9

SCOPUS: 2-s2.0-77952878970

Wos: WOS:000240128100011

Source Identifiers

ISSN: 1434-5161

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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

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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

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