Molecular genetics of PKU in eastern Europe: a nonsense mutation associated with haplotype 4 of the phenylalanine hydroxylase gene

scientific article published on 01 January 1990

Molecular genetics of PKU in eastern Europe: a nonsense mutation associated with haplotype 4 of the phenylalanine hydroxylase gene is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/BF01650483
P698PubMed publication ID2309142

P2093author name stringWang T
Woo SL
Fekete G
Berencsi G
Okano Y
Eisensmith RC
Schuler D
Nasz I
P433issue1
P921main subjectEastern EuropeQ27468
molecular geneticsQ210506
P304page(s)85-90
P577publication date1990-01-01
P1433published inSomatic Cell and Molecular GeneticsQ7559232
P1476titleMolecular genetics of PKU in eastern Europe: a nonsense mutation associated with haplotype 4 of the phenylalanine hydroxylase gene
P478volume16

Reverse relations

cites work (P2860)
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Q39585151A missense mutation, S349P, completely inactivates phenylalanine hydroxylase in north African Jews with phenylketonuria
Q70177711A prevalent missense mutation in Northern Europe associated with hyperphenylalaninaemia
Q67526310Analysis of exon 7 of the human phenylalanine hydroxylase gene: a mutation hot spot?
Q37548966Clinical application of genotypic diagnosis for phenylketonuria: theoretical considerations
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Q37427817Founder effect of a prevalent phenylketonuria mutation in the Oriental population
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Q71589721Phenylketonuria genotypes correlated to metabolic phenotype groups in Norway
Q72033695Phenylketonuria in China: identification and characterization of three novel nucleotide substitutions in the human phenylalanine hydroxylase gene
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Q70587638Relation between genotype and phenotype in Swedish phenylketonuria and hyperphenylalaninemia patients
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