Sequence variation at the phenylalanine hydroxylase gene in the British Isles

American Journal of Human Genetics

Volumn 60, Issue 2, 1997, Pages 388-396

  Tyfield, L A ^a,b   Stephenson, A ^a   Cockburn, F ^c   Harvie, A ^c   Bidwell, J L ^b   Wood, N A P ^b   Pilz, D T ^d   Harper, P ^d   Smith, I ^e  

^a SOUTHMEAD HOSPITAL   (United Kingdom)

^b UNIVERSITY OF BRISTOL   (United Kingdom)

^c ROYAL HOSPITAL FOR SICK CHILDREN   (United Kingdom)

^d CARDIFF UNIVERSITY   (United Kingdom)

^e UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE 4 MONOOXYGENASE;

AMINO ACID METABOLISM; ARTICLE; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENETIC HETEROGENEITY; GENETIC VARIABILITY; GEOGRAPHIC DISTRIBUTION; HAPLOTYPE; HUMAN; HUMAN TISSUE; PHENYLKETONURIA; POPULATION RESEARCH; PRIORITY JOURNAL;

ALLELES; CLUSTER ANALYSIS; DNA MUTATIONAL ANALYSIS; ENGLAND; EXONS; HAPLOTYPES; HUMANS; MINISATELLITE REPEATS; MUTATION; NUCLEIC ACID HETERODUPLEXES; PHENYLALANINE HYDROXYLASE; PHENYLKETONURIAS; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SCOTLAND; VARIATION (GENETICS); WALES;

EID: 0031020421     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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