Novel truncating SF1 gene variant in a family with mild neurodevelopmental disorder: expanding the phenotype of SF1-related spliceosomopathy spectrum
A unique familial case of a novel truncating variant in a single Czech family presenting with mild neurodevelopmental disorders (NDD) and variable congenital abnormalities is reported, expanding the spectrum of pathogenic variants involved in the development of new SF1 -related spliceosomopathy and its diverse phenotyp...