Molecular genetics of peroxidase deficiency

Journal of Molecular Medicine

Volumn 76, Issue 10, 1998, Pages 688-698

  Petrides, Petro E ^a,b,c,d  

^a UNIVERSITY OF MUNICH   (Germany)

^b SALK INSTITUTE FOR BIOLOGICAL STUDIES   (United States)

^c STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d HUMBOLDT UNIVERSITY   (Germany)

Author keywords

Genotype phenotype relationship; Mutation analysis; Peroxidase deficiency

Indexed keywords

LACTOPEROXIDASE; MYELOPEROXIDASE; PEROXIDASE;

ALLELE; DNA SEQUENCE; ENZYME DEFICIENCY; GENE EXPRESSION REGULATION; GENE MUTATION; GENE STRUCTURE; GENOTYPE; HUMAN; LEUKEMIA; MOLECULAR GENETICS; MULTIGENE FAMILY; PHENOTYPE; REVIEW; TRANSCRIPTION REGULATION;

AMINO ACID SEQUENCE; BASE SEQUENCE; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HUMANS; MALE; METABOLISM, INBORN ERRORS; MOLECULAR SEQUENCE DATA; MULTIGENE FAMILY; PEROXIDASE; PHENOTYPE;

EID: 0031659445     PISSN: 09462716     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001090050269     Document Type: Review

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