A new type of inherited catalase deficiencies: Its characterization and comparison to the Japanese and Swiss type of acatalasemia

Blood Cells, Molecules, and Diseases

Volumn 27, Issue 2, 2001, Pages 512-517

  Góth, László ^a  

^a UNIVERSITY OF DEBRECEN   (Hungary)

Author keywords

Acatalasemia; Catalase; Hungarian; Hypocatalasemia; Mutation

Indexed keywords

CATALASE; HYDROGEN PEROXIDE;

ADULT; AMINO ACID SUBSTITUTION; ATHEROSCLEROSIS; BLOOD LEVEL; CARBOHYDRATE METABOLISM; CATALASE DEFICIENCY; CONFERENCE PAPER; CONTROLLED STUDY; DIABETES MELLITUS; ENZYME ACTIVITY; ETHNIC GROUP; EXON; EXPOSURE; FEMALE; GENE INSERTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC SCREENING; HUMAN; HUNGARY; INCIDENCE; INTRON; JAPAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RISK FACTOR;

EID: 0034976899     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1006/bcmd.2001.0415     Document Type: Conference Paper

References (31)

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27. Further characterization of Hungarian acatalasemia by Hinf 1 polymorphism of catalase gene
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