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.
about
A multidimensional approach to an in-depth proteomics analysis of transcriptional regulators in neuroblastoma cellsRecent advances in genetics of choreaMovement disorders in spinocerebellar ataxias.Huntington's disease phenocopies are clinically and genetically heterogeneous.Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion.
P2860
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.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Exclusion of mutations in the ...... h a Huntington-like phenotype.
@ast
Exclusion of mutations in the ...... h a Huntington-like phenotype.
@en
Exclusion of mutations in the ...... h a Huntington-like phenotype.
@nl
type
label
Exclusion of mutations in the ...... h a Huntington-like phenotype.
@ast
Exclusion of mutations in the ...... h a Huntington-like phenotype.
@en
Exclusion of mutations in the ...... h a Huntington-like phenotype.
@nl
prefLabel
Exclusion of mutations in the ...... h a Huntington-like phenotype.
@ast
Exclusion of mutations in the ...... h a Huntington-like phenotype.
@en
Exclusion of mutations in the ...... h a Huntington-like phenotype.
@nl
P2093
P2860
P50
P1476
Exclusion of mutations in the ...... h a Huntington-like phenotype.
@en
P2093
Conceição Robalo
Célia Barbosa
Joana Cerqueira
José Barros
Manuela M Santos
Marina Magalhães
Paula Magalhães
Vitorina Passão
P2860
P2888
P304
P356
10.1007/S10038-006-0001-9
P50
P577
2006-07-21T00:00:00Z