Early neurological phenotype in 4 children with biallelic PRODH mutations
about
Functional polymorphisms in PRODH are associated with risk and protection for schizophrenia and fronto-striatal structure and functionEvidence for association of hyperprolinemia with schizophrenia and a measure of clinical outcomeMecp2-null mice provide new neuronal targets for Rett syndrome.Physical manifestations of neurodevelopmental disruption: are minor physical anomalies part of the syndrome of schizophrenia?Safety of L-proline as a stabilizer for immunoglobulin products.An environmental analysis of genes associated with schizophrenia: hypoxia and vascular factors as interacting elements in the neurodevelopmental model.The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD.Biochemical and clinical features of hereditary hyperprolinemia.Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2.Molecular genetics of 22q11.2 deletion syndrome
P2860
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P2860
Early neurological phenotype in 4 children with biallelic PRODH mutations
description
2007 nî lūn-bûn
@nan
2007 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Early neurological phenotype in 4 children with biallelic PRODH mutations
@ast
Early neurological phenotype in 4 children with biallelic PRODH mutations
@en
Early neurological phenotype in 4 children with biallelic PRODH mutations
@nl
type
label
Early neurological phenotype in 4 children with biallelic PRODH mutations
@ast
Early neurological phenotype in 4 children with biallelic PRODH mutations
@en
Early neurological phenotype in 4 children with biallelic PRODH mutations
@nl
prefLabel
Early neurological phenotype in 4 children with biallelic PRODH mutations
@ast
Early neurological phenotype in 4 children with biallelic PRODH mutations
@en
Early neurological phenotype in 4 children with biallelic PRODH mutations
@nl
P2093
P1476
Early neurological phenotype in 4 children with biallelic PRODH mutations
@en
P2093
Agnés Guët
Alexandra Afenjar
Anne-Isabelle Vermersch
Cyril Mignot
Daniel Rabier
Delphine Heron
Diana Rodriguez
Diane Doummar
Elizabeth Thioulouse
Lydie Burglen
P304
P356
10.1016/J.BRAINDEV.2007.01.008
P407
P577
2007-10-01T00:00:00Z