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Volumn 525, Issue 2, 2012, Pages 201-206

A simple method for examination of polymorphisms of catalase exon 9: Rs769217 in Hungarian microcytic anemia and beta-thalassemia patients

(4) Nagy, Teréz a Csordás, Melinda a Kósa, Zsuzsanna a Góth, László a

a UNIVERSITY OF DEBRECEN (Hungary)

Author keywords

Acatalasemia; Beta thalassemia; Catalase gene mutations screening; Microcytic anemia; SSCP

Indexed keywords

CATALASE; ETHIDIUM BROMIDE; NUCLEASE; SINGLE STRANDED DNA;

ADULT; AMPLICON; ARTICLE; BASE PAIRING; BETA THALASSEMIA; CATALASE DEFICIENCY; CONTROLLED STUDY; DNA DENATURATION; DNA POLYMORPHISM; ENZYME ACTIVITY; EXON; FEMALE; GEL ELECTROPHORESIS; GENE MUTATION; GENE SEQUENCE; GENE STRUCTURE; GENETIC ASSOCIATION; GENETIC PROCEDURES; GENETIC SCREENING; GENOTYPE; HUMAN; HUMAN TISSUE; HUNGARY; MAJOR CLINICAL STUDY; MALE; MICROCYTIC ANEMIA; MOLECULAR DIAGNOSIS; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEQUENCE ANALYSIS; SILVER STAINING; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADOLESCENT; ADULT; ANEMIA; BETA-THALASSEMIA; CATALASE; EXONS; FEMALE; GENOTYPE; HUMANS; HUNGARY; MALE; MIDDLE AGED; MODELS, GENETIC; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEQUENCE ANALYSIS, DNA;

EID: 84864613582 PISSN: 00039861 EISSN: 10960384 Source Type: Journal
DOI: 10.1016/j.abb.2012.01.004 Document Type: Article

Times cited : (5)

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