A very rare case report of glycogen storage disease type IXc with novel PHKG2 variants.

Name: A very rare case report of glycogen storage disease type IXc with novel PHKG2 variants.
Author: Shao, Yongxian

A very rare case report of glycogen storage disease type IXc with novel PHKG2 variants. — المؤلف: Shao, Yongxian — BMC pediatrics 20220517

المؤلف: Shao, Yongxian
النشر: BMC pediatrics 20220517
الوصف: 267 p.
الموضوعات: Glycogen Storage Disease؛ Humans؛ Hypoglycemia؛ Infant, Newborn؛ Liver؛ Mutation؛ Phosphorylase Kinase