Novel point mutation in exon 12 of the glucose-6- Phosphate Dehydrogenase Gene: G6PD Flores

This publication has 9 references indexed in Scilit:

• Glucose-6-phosphate Dehydrogenase Deficiency in Portugal: Biochemical and Mutational Profiles, Heterogeneity, and Haplotype Association
  Blood Cells, Molecules, and Diseases, 2002
• G6PDdb, an integrated database of glucose-6-phosphate dehydrogenase (G6PD) mutations
  Human Mutation, 2002
• Consanguinity, cardiac arrest, hearing impairment, and ECG abnormalities: counselling pitfalls in the Romano-Ward syndrome.
  Journal of Medical Genetics, 1993
• Hereditary anaemias in Portugal: epidemiology, public health significance, and control.
  Journal of Medical Genetics, 1993
• Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene
  Human Mutation, 1993
• The molecular basis of glucose-6-phosphate dehydrogenase deficiency
  Trends in Genetics, 1992
• The genetics of glucose-6-phosphate dehydrogenase deficiency.
  1990
• A simple salting out procedure for extracting DNA from human nucleated cells
  Nucleic Acids Research, 1988
• DNA sequencing with chain-terminating inhibitors
  Proceedings of the National Academy of Sciences, 1977