Publicações

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)

Indexing

Wos^®

Scopus^®

Crossref^®

Google Scholar^®

Publication Identifiers

DOI: 10.1007/s10038-006-0001-9

SCOPUS: 2-s2.0-77952878970

Wos: WOS:000240128100011

Source Identifiers

ISSN: 1434-5161

Export Publication Metadata

Lista Marked

Adicionar à lista Marked

Citações

Oops! It looks like you don't have access to this content.

This section is restricted to uses with b-on access.

CORE Conference

No information about CORE Rank

During the preprocessing phase, only publications of type 'Proceedings Paper' or 'Proceedings' are automatically processed to identify their CORE Rank.

TIP: If your publication's CORE Rank is missing, you can contact with your institutional manager to have the correct ranking manually added to the record.

Journal Factors

Oops! It looks like you don't have access to this content.

This section is restricted to uses with b-on access.

Full Text

Full Text @ sfx.b-on.pt

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

Links Úteis

Ajuda

Autenticação Federada (Clique na imagem)

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

Links Úteis

Ajuda