A case of combined oxidative phosphorylation deficiency 32 caused by MRPS34 gene variation and literature review

von Shen, M X
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2023)

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 characteristics of epileptic seizure in neurofibromatosis type 1 in 15 cases

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

Research progress on DEPDC5 gene related epilepsy

von Shen, M X
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2022)

ACTG2 associated visceral myopathy with intestinal pseudoobstruction

von Shen, M X
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2021)