Phenylketonuria mutations and linked haplotypes in the lithuanian population: Origin of the most common R408W mutation

Human Heredity

Volumn 47, Issue 3, 1997, Pages 155-160

  Giannattasio, S ^a   Jurgelevicius V ^b   Lattanzio, P ^a   Cimbalistiene L ^b   Marra, E ^a   Kucinskas V ^b  

^a CNR   (Italy)

^b VILNIUS UNIVERSITY   (Lithuania)

Author keywords

Lithuanian population; Minihaplotypes (VNTR and STR); Phenylalanine hydroxylase mutations; Phenylketonuria

Indexed keywords

PHENYLALANINE 4 MONOOXYGENASE;

ALLELE; ARTICLE; CONTROLLED STUDY; GENE FREQUENCY; GENE MUTATION; GENEALOGY; HAPLOTYPE; HUMAN; LITHUANIA; MAJOR CLINICAL STUDY; PHENYLKETONURIA; TANDEM REPEAT; VARIABLE NUMBER OF TANDEM REPEAT;

EID: 1842288054     PISSN: 00015652     EISSN: 14230062     Source Type: Journal    
DOI: 10.1159/000154403     Document Type: Article

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