Recurrent mutation in the human phenylalanine hydroxylase gene.

समान संसाधन

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