NRXN1, neurexin 1, 9378

N. diseases: 139; N. variants: 41
Disease: Asperger Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0236792
Disease: Asperger Syndrome
Asperger Syndrome 		0.010 GeneticVariation disease BEFREE Mutations in NLGN3/4, SHANK3, or NRXN1 alter synaptic function and lead to mental retardation, typical autism, or Asperger syndrome. 19545994 2009