[Clinical and genetic characteristics of children with STXBP1 encephalopathy]

Authors :: J J, Cao
X N, Ji
Y Y, Mao
P P, Zhang
W T, Liu
H Z, Zhang
N, Ding
Q, Chen
Source :: Zhonghua er ke za zhi = Chinese journal of pediatrics. 58(6)
Publication Year :: 2020

Subjects :: Male
Brain Diseases
Epilepsy
Developmental Disabilities
Infant
Electroencephalography
Munc18 Proteins
Child, Preschool
Mutation
Humans
Point Mutation
Female
Spasms, Infantile
Retrospective Studies

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