Studies on Hypoxanthine-Guanine Phosphoribosyltransferase in Fibroblasts from Patients with the Lesch-Nyhan Syndrome

Míreanna comhchosúla

• Hypoxanthine-guanine phosphoribosyltransferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome
  de réir: Arnold, William J., et al.
  Foilsithe / Cruthaithe: (1972)
• Hypoxanthine-guanine phosphoribosyltransferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome
  de réir: William J. Arnold, et al.
  Foilsithe / Cruthaithe: (1972)
• Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in a patient with the Lesch-Nyhan syndrome.
  de réir: Wilson, J M, et al.
  Foilsithe / Cruthaithe: (1983)
• Identification of a single nucleotide change in the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTYale) responsible for Lesch-Nyhan syndrome.
  de réir: Fujimori, S, et al.
  Foilsithe / Cruthaithe: (1989)
• Molecular analysis of hypoxanthine guanine phosphoribosyltransferase (HPRT) gene in five Korean families with Lesch-Nyhan syndrome.
  de réir: Kim, K. J., et al.
  Foilsithe / Cruthaithe: (1997)