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

被引：0
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作者：
Yongxian Shao
Taolin Li
Minyan Jiang
Jianan Xu
Yonglan Huang
Xiuzhen Li
Ruidan Zheng
Li Liu
机构：
[1] Guangzhou Medical University,Department of Pediatric Endocrinology and Genetic Metabolism, Guangzhou Women and Children’s Medical Center
来源：
BMC Pediatrics | / 22卷
关键词：
Glycogen storage disease; Phosphorylase b kinase; Case report;
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