Association between minihaplotypes and mutations at the PAH locus in Polish hyperphenylalaninemic patients

Human Heredity

Volumn 51, Issue 1-2, 2001, Pages 117-120

  Zekanowski, Cezary ^a   Jurkowska, Monika ^a   Bal, Jerzy ^a  

^a INSTITUTE OF MOTHER AND CHILD   (Poland)

Author keywords

Hyperphenylalaninemia; Minihaplotypes; Mutations; PAH; Phenylketonuria; Polish population; Polymorphis m

Indexed keywords

AMINO ACID; PHENYLALANINE 4 MONOOXYGENASE;

ALLELE; ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE SEVERITY; GENE LOCUS; GENE MUTATION; GENETIC VARIABILITY; GEOGRAPHIC DISTRIBUTION; HAPLOTYPE; HUMAN; HYPERPHENYLALANINEMIA; MAJOR CLINICAL STUDY; PHENOTYPE; PHENYLKETONURIA; POLAND; TANDEM REPEAT; VARIABLE NUMBER OF TANDEM REPEAT;

HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MUTATION; PHENYLALANINE HYDROXYLASE; PHENYLKETONURIAS; POLAND; POLYMORPHISM, GENETIC; TANDEM REPEAT SEQUENCES;

EID: 0035205479     PISSN: 00015652     EISSN: None     Source Type: Journal    
DOI: 10.1159/000022951     Document Type: Article

References (21)

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