Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder.

J Autism Dev Disord

Departamento de Bioquímica y Medicina Molecular, Facultad de Medicina, Universidad Autónoma de Nuevo León, Av. Fco. I. Madero s/n, Mitras Centro, Monterrey, Nuevo León, Mexico.

Published: June 2020

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http://dx.doi.org/10.1007/s10803-019-03951-zDOI Listing

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