Further delineation of the SCAF4-associated neurodevelopmental disorderCosima M. Schmid, Małgorzata J.M. Nowaczyk, Isabella Herman et al.|European Journal of Human Genetics|2024Cited by 5
Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome’s clinical and molecular spectrum through NALCN in-silico structural analysisDavide Vecchio, Tommaso Mazza, Marina Macchiaiolo et al.|Frontiers in Genetics|2024Cited by 2