Molecular biology of phenylketonuria
- PMID: 2891509
- DOI: 10.1007/BF00442048
Molecular biology of phenylketonuria
Similar articles
-
The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations.Hum Genet. 1991 Aug;87(4):377-88. doi: 10.1007/BF00197152. Hum Genet. 1991. PMID: 1679029 Review.
-
[Phenylketonuria].Tanpakushitsu Kakusan Koso. 1988 Apr;33(5):487-92. Tanpakushitsu Kakusan Koso. 1988. PMID: 2908394 Japanese. No abstract available.
-
Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families.Hum Genet. 1991 May;87(1):11-7. doi: 10.1007/BF01213084. Hum Genet. 1991. PMID: 1674714
-
Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria.J Pediatr. 1987 Jan;110(1):68-71. doi: 10.1016/s0022-3476(87)80290-1. J Pediatr. 1987. PMID: 2878985
-
Molecular basis and population genetics of phenylketonuria.Biochemistry. 1989 Jan 10;28(1):1-7. doi: 10.1021/bi00427a001. Biochemistry. 1989. PMID: 2565120 Review. No abstract available.
Cited by
-
The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuria.Hum Genet. 1991 Jan;86(3):247-50. doi: 10.1007/BF00202402. Hum Genet. 1991. PMID: 1671768
-
The influence of mutations of enzyme activity and phenylalanine tolerance in phenylalanine hydroxylase deficiency.Eur J Pediatr. 1996 Jul;155 Suppl 1:S6-10. doi: 10.1007/pl00014253. Eur J Pediatr. 1996. PMID: 8828600 Review.
-
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy.Hum Genet. 1990 Nov;86(1):69-72. doi: 10.1007/BF00205176. Hum Genet. 1990. PMID: 1979309
-
The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations.Hum Genet. 1991 Aug;87(4):377-88. doi: 10.1007/BF00197152. Hum Genet. 1991. PMID: 1679029 Review.
-
Mouse models of human phenylketonuria.Genetics. 1993 Aug;134(4):1205-10. doi: 10.1093/genetics/134.4.1205. Genetics. 1993. PMID: 8375656 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Medical