Associated Papers
Clinical and genetic analyses of 17 Chinese patients with glycogen storage disease type IXc.
Sun C et al.
Orphanet Journal of Rare Diseases, 2025
Glycogen storage disorder types IX: the mutation spectrum and ethnic distribution.
Geramizadeh B et al.
Orphanet Journal of Rare Diseases, 2024
A very rare case report of glycogen storage disease type IXc with novel PHKG2 variants.
Shao Y et al.
Bmc Pediatrics, 2022
Glycogen storage diseases: Twenty-seven new variants in a cohort of 125 patients.
Sperb-Ludwig F et al.
Molecular Genetics & Genomic Medicine, 2019
Novel PHKG2 mutation causing GSD IX with prominent liver disease: report of three cases and review of literature.
Albash B et al.
European Journal of Pediatrics, 2014
Select a paper to view details