A novel mutation in KCNB1 gene in a child with neuropsychiatric comorbidities with both intellectual disability and epilepsy and review of literature

von Miao, P
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2017)

A childhood-onset rapid-onset dystonia parkinsonism family with ATP1A3 gene mutation and literatures review

von Zhang, C L
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2017)