Hypoxanthine-guanine phosphoribosyltransferase. Genetic evidence for identical mutations in two partially deficient subjects.

Gelijkaardige items

• A molecular survey of hypoxanthine-guanine phosphoribosyltransferase deficiency in man.
  door: Wilson, J M, et al.
  Gepubliceerd in: (1986)
• Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in ten subjects determined by direct sequencing of amplified transcripts.
  door: Davidson, B L, et al.
  Gepubliceerd in: (1989)
• Identification of 17 independent mutations responsible for human hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency.
  door: Davidson, B L, et al.
  Gepubliceerd in: (1991)
• Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in a patient with the Lesch-Nyhan syndrome.
  door: Wilson, J M, et al.
  Gepubliceerd in: (1983)
• Hypoxanthine-guanine phosphoribosyltransferase deficiency and Xg blood group.
  door: Greene, M L, et al.
  Gepubliceerd in: (1970)