Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations

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Authors

Marina Konyukh · Gènes, synapses et cognition

Richard Delorme · Assistance Publique – Hôpitaux de Paris

Pauline Chaste · Gènes, synapses et cognition

Claire S. Leblond · Gènes, synapses et cognition

Nathalie Lemière · Institut Pasteur

Gudrun Nygren · University of Gothenburg

Henrik Anckarsäter

Abstract

Our results provide an extensive ascertainment of the genetic variability of SEZ6L2 in human populations and do not support a major role for SEZ6L2 sequence variations in the susceptibility to ASD.

Topics & Keywords

Genomic variations and chromosomal abnormalities Autism Spectrum Disorder Research Genetics and Neurodevelopmental Disorders

Publication Details

Published in: PLoS ONE

Volume 6, Issue 3, pp. e17289-e17289

DOI: 10.1371/journal.pone.0017289

Field-Weighted Citation Impact: 1.57

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Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations

Authors

Abstract

Topics & Keywords

Publication Details