Molecular genetic analysis of glycogen storage disease type Ia in 26 Chinese patients

J Inherit Metab Dis. 2003;26(8):811-2. doi: 10.1023/b:boli.0000009992.78840.77.

Abstract

Sequence analysis of 26 patients from Mainland China with glycogen storage disease type Ia revealed a high frequency of two mutations in the glucose-6-phosphatase gene. These mutations, 727G>T and R83H, were also found to be in linkage disequilibrium with a polymorphism at position 1176. These findings have implications for carrier detection and prenatal diagnosis of this disease in the Chinese population.

MeSH terms

  • Asian People
  • Glucose-6-Phosphatase / genetics*
  • Glycogen Storage Disease Type I / genetics*
  • Humans
  • Mutation*

Substances

  • Glucose-6-Phosphatase