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

The American Journal of Human Genetics · 2004 · Vol. 74(3) · pp. 552–557
Frédéric LaumonnierFrédérique Bonnet‐BrilhaultMarie GomotRomuald BlancAlbert DavidMarie‐Pierre MoizardMartine RaynaudNathalie RonceÉric LemonnierPatrick CalvasBéatrice LaudierJamel ChellyJean‐Pierre FrynsHans‐Hilger RopersBen C.J. HamelChristian AndrésCatherine BarthélémyClaude MoraineSylvain Briault
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalitiesNeuroliginNeurexinAutismGeneticsMutationGeneSynaptogenesisBiologyStop codonPsychology

MeSH terms

AdolescentAdultAutistic DisorderCarrier ProteinsChildChild, PreschoolFemaleHumansGenetic LinkageMaleMembrane ProteinsMutationPedigreeCell Adhesion Molecules, NeuronalX-Linked Intellectual Disability
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