X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family-Reference-Cited by-同舟云学术

X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

Published:2004-03 Issue:3 Volume:74 Page:552-557
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Laumonnier Frédéric,Bonnet-Brilhault Frédérique,Gomot Marie,Blanc Romuald,David Albert,Moizard Marie-Pierre,Raynaud Martine,Ronce Nathalie,Lemonnier Eric,Calvas Patrick,Laudier Béatrice,Chelly Jamel,Fryns Jean-Pierre,Ropers Hans-Hilger,Hamel Ben C.J.,Andres Christian,Barthélémy Catherine,Moraine Claude,Briault Sylvain

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. Diagnostic and statistical manual of mental disorders;American Psychiatric Association,1994

2. A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25–27;Auranen;Am J Hum Genet,2002

3. ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation;Bienvenu;Hum Mol Genet,2002

4. Identification of a novel neuroligin in humans which binds to PSD-95 and has a widespread expression;Bolliger;Biochem J,2001

5. A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation;Carrie;Nat Genet,1999

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