A novel DraI polymorphism in the 3' untranslated region of human glucose-6-phosphatase gene: useful for carrier detection and prenatal diagnosis of glycogen storage disease type 1a

Clin Genet. 1998 Jun;53(6):502-3. doi: 10.1111/j.1399-0004.1998.tb02604.x.
No abstract available

MeSH terms

  • Base Sequence
  • Chromosome Mapping
  • DNA, Complementary
  • Deoxyribonucleases, Type II Site-Specific
  • Genetic Markers
  • Glucose-6-Phosphatase / genetics*
  • Glycogen Storage Disease / enzymology*
  • Glycogen Storage Disease / genetics
  • Heterozygote*
  • Humans
  • Molecular Sequence Data
  • Nucleic Acid Hybridization
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Prenatal Diagnosis*
  • Protein Biosynthesis
  • Restriction Mapping

Substances

  • DNA, Complementary
  • Genetic Markers
  • Deoxyribonucleases, Type II Site-Specific
  • TTTAAA -specific type II deoxyribonucleases
  • Glucose-6-Phosphatase

Associated data

  • GENBANK/U01120