Vitobello A et al. ADGRL1 haploinsufficiency causes a variable spectrum of neurodevelopmental disorders in humans and alters synaptic activity and behavior in a mouse model. Am J Hum Genet. 2022 Aug 4;109(8):1436-1457. PMID: 35907405.
Guo H et al. Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes.Genet Med. 2019 Jul;21(7):1611-1620. PMID: 30504930.
Meza-Aguilar DG et al. Latrophilins updated.Biomol Concepts. 2014 Dec;5(6):457-78. PMID: 25429599.
