Recurrent mutation in the human phenylalanine hydroxylase gene.

Схожие документы

• Missense mutations associated with RFLP haplotypes 1 and 4 of the human phenylalanine hydroxylase gene.
  по: Okano, Y, et al.
  Опубликовано: (1990)
• Associations between mutations and a VNTR in the human phenylalanine hydroxylase gene.
  по: Goltsov, A A, et al.
  Опубликовано: (1992)
• Molecular genetics of phenylketonuria in Orientals: linkage disequilibrium between a termination mutation and haplotype 4 of the phenylalanine hydroxylase gene.
  по: Wang, T, et al.
  Опубликовано: (1989)
• Recurrent mutation, gene conversion, or recombination at the human phenylalanine hydroxylase locus: evidence in French-Canadians and a catalog of mutations.
  по: John, S W, et al.
  Опубликовано: (1990)
• Updated listing of haplotypes at the human phenylalanine hydroxylase (PAH) locus.
  по: Eisensmith, R C, et al.
  Опубликовано: (1992)