Fig. 2From: The recurrent WASF1 nonsense variant identified in two unaffected Chinese families with neurodevelopmental disorder: case report and review of the literatures A The pedigree of the two families. The de novo variant WASF1:c.1516 C > T is identified in two Chinese families respectively. B Distribution of truncation variants included in HGMD database in WASF1 protein domain patternBack to article page