NLGN4X, neuroligin 4 X-linked, 57502

N. diseases: 45; N. variants: 18
Disease: Pervasive Development Disorder ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.030 GeneticVariation group BEFREE Two specific point mutations in NLGN3 and NLGN4 genes, involved in autistic spectrum disorder, were further characterized in this experimental system. 22723984 2012
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.030 GeneticVariation group BEFREE We conclude that there is no evidence for an involvement of NLGN3 and NLGN4X genetic variants with autism spectrum disorder on high functioning level in our study group. 18189281 2008
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.030 GeneticVariation group BEFREE A large French family including members affected by nonspecific X-linked mental retardation, with or without autism or pervasive developmental disorder in affected male patients, has been found to have a 2-base-pair deletion in the Neuroligin 4 gene (NLGN4) located at Xp22.33. 14963808 2004