The spectrum of mutations and methods for their detection in the phenylalanine hydroxylase gene in phenylketonuria patients from the novosibirsk region

Bioorganicheskaya Khimiya

Volumn 26, Issue 11, 2000, Pages 838-843

  Smagulova, F O ^a   Morozov, I V ^a  

^a INSTITUTE OF CHEMICAL BIOLOGY AND FUNDAMENTAL MEDICINE   (Russian Federation)

Author keywords

ACRS PCR; DGGE; Mutations; Phenylalanine hydroxylase; Phenylketonuria

Indexed keywords

PHENYLALANINE 4 MONOOXYGENASE;

ARTICLE; ENZYMOLOGY; GENE DELETION; GENETICS; HUMAN; MISSENSE MUTATION; PHENYLKETONURIA; POINT MUTATION; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

HUMANS; MUTATION, MISSENSE; PHENYLALANINE HYDROXYLASE; PHENYLKETONURIAS; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SEQUENCE DELETION;

EID: 0040748487     PISSN: 01323423     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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