Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.

Benzer Materyaller

• Glucose-6-Phosphate Dehydrogenase and Hemolytic Anemia
  Baskı/Yayın Bilgisi: (1962)
• Specific methylation pattern at the 3' end of the human housekeeping gene for glucose 6-phosphate dehydrogenase.
  Yazar:: Toniolo, D, ve diğerleri
  Baskı/Yayın Bilgisi: (1984)
• Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase.
  Yazar:: Martini, G, ve diğerleri
  Baskı/Yayın Bilgisi: (1986)
• Tissue-specific levels of human glucose-6-phosphate dehydrogenase correlate with methylation of specific sites at the 3' end of the gene.
  Yazar:: Battistuzzi, G, ve diğerleri
  Baskı/Yayın Bilgisi: (1985)
• Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA.
  Yazar:: Poggi, V, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)