A case of intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures caused by PHF21A gene variation and review of lite...

von Wu, F
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2023)

Clinical and genetic characteristics of children with STXBP1 encephalopathy

von Cao, J J
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2020)