Rare NRXN1 promoter variants in patients with schizophrenia
about
Deletion of glutamate delta-1 receptor in mouse leads to aberrant emotional and social behaviorsNeurexin-1 and frontal lobe white matter: an overlapping intermediate phenotype for schizophrenia and autism spectrum disordersSelected rapporteur summaries from the XX World Congress of Psychiatric Genetics, Hamburg, Germany, October 14-18, 2012.Sex-dependent novelty response in neurexin-1α mutant mice.The genetics of Tourette disorderMolecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs.Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature.Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes.
P2860
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P2860
Rare NRXN1 promoter variants in patients with schizophrenia
description
2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
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2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
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name
Rare NRXN1 promoter variants in patients with schizophrenia
@ast
Rare NRXN1 promoter variants in patients with schizophrenia
@en
type
label
Rare NRXN1 promoter variants in patients with schizophrenia
@ast
Rare NRXN1 promoter variants in patients with schizophrenia
@en
prefLabel
Rare NRXN1 promoter variants in patients with schizophrenia
@ast
Rare NRXN1 promoter variants in patients with schizophrenia
@en
P2093
P2860
P1433
P1476
Rare NRXN1 promoter variants in patients with schizophrenia
@en
P2093
Abhishek K Shah
Catalina Villa
Erika Pedrosa
Herbert M Lachman
Joseph Locker
Karen Nolan
Katherine Groh
Nina M Tioleco
Pavla Stopkova
P2860
P356
10.1016/J.NEULET.2010.03.047
P407
P577
2010-03-25T00:00:00Z