Identification of a novel mutation (867delA) in the glucose-6-phosphatase gene in two siblings with glycogen storage disease type Ia with different phenotypes

Hum Mutat. 2000 Apr;15(4):381. doi: 10.1002/(SICI)1098-1004(200004)15:4<381::AID-HUMU13>3.0.CO;2-K.

Abstract

We identified a novel mutation (867delA) in the glucose-6-phosphatase gene of two siblings with glycogen storage disease type Ia. Although both siblings share the same mutations, their phenotype regarding adult height and hepatomegaly differs. In glycogen storage disease type Ia, substantial heterogeneity in phenotype is observed. So far, no evidence for a clear genotype-phenotype correlation has been found. Hum Mutat 15:381, 2000.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Exons / genetics
  • Female
  • Frameshift Mutation*
  • Genotype
  • Glucose-6-Phosphatase / genetics*
  • Glycogen Storage Disease / enzymology*
  • Glycogen Storage Disease / genetics*
  • Humans
  • Male
  • Nuclear Family
  • Phenotype
  • Polymorphism, Single-Stranded Conformational

Substances

  • Glucose-6-Phosphatase