Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
About this item
Full title
Author / Creator
Gauthier, Julie , Siddiqui, Tabrez J. , Huashan, Peng , Yokomaku, Daisaku , Hamdan, Fadi F. , Champagne, Nathalie , Lapointe, Mathieu , Spiegelman, Dan , Noreau, Anne , Lafrenière, Ronald G. , Fathalli, Ferid , Joober, Ridha , Krebs, Marie-Odile , DeLisi, Lynn E. , Mottron, Laurent , Fombonne, Éric , Michaud, Jacques L. , Drapeau, Pierre , Carbonetto, Salvatore , Craig, Ann Marie and Rouleau, Guy A.
Publisher
Berlin/Heidelberg: Springer-Verlag
Journal title
Language
English
Formats
Publication information
Publisher
Berlin/Heidelberg: Springer-Verlag
Subjects
More information
Scope and Contents
Contents
Growing genetic evidence is converging in favor of common pathogenic mechanisms for autism spectrum disorders (ASD), intellectual disability (ID or mental retardation) and schizophrenia (SCZ), three neurodevelopmental disorders affecting cognition and behavior. Copy number variations and deleterious mutations in synaptic organizing proteins includi...
Alternative Titles
Full title
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
Authors, Artists and Contributors
Author / Creator
Siddiqui, Tabrez J.
Huashan, Peng
Yokomaku, Daisaku
Hamdan, Fadi F.
Champagne, Nathalie
Lapointe, Mathieu
Spiegelman, Dan
Noreau, Anne
Lafrenière, Ronald G.
Fathalli, Ferid
Joober, Ridha
Krebs, Marie-Odile
DeLisi, Lynn E.
Mottron, Laurent
Fombonne, Éric
Michaud, Jacques L.
Drapeau, Pierre
Carbonetto, Salvatore
Craig, Ann Marie
Rouleau, Guy A.
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3204930
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3204930
Other Identifiers
ISSN
0340-6717
E-ISSN
1432-1203
DOI
10.1007/s00439-011-0975-z
