Amarillo I

References (1)

Title : Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization - Kopp_2020_Am.J.Med.Genet.A__e62025
Author(s) : Kopp N , Amarillo I , Martinez-Agosto J , Quintero-Rivera F
Ref : American Journal of Medicine Genet A , :e62025 , 2020
PubMedID: 33369065
Gene_locus related to this paper: human-NLGN4X