Sodium taurocholate cotransporter polypeptide deficiency combined with novel PYGL mutations in glycogen storage disease type VI: a rare case report

Clinics and Research in Hepatology and Gastroenterology 2026

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Authors: Meifen Wang, Mingying Wang, Juan Li, Rui Chen, Zhongrui Bi, Hongchao Jiang, Jiwei Li

DOI: 10.1016/j.clinre.2026.102801

Cited by: 0

References: 14

Fields of Study & Subjects

Glycogen Storage Diseases and Myoclonus Metabolism and Genetic Disorders Pediatric Hepatobiliary Diseases and Treatments

References 14