Case Report-An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions.
René Günther FeichtingerMartin PreiselKarin BruggerSaskia B WortmannJohannes Adalbert MayrPublished in: Genes (2023)
as a novel gene for neurodevelopmental disorders with autism.