Coexistence of Deficiencies of Uroporphyrinogen III Synthase and Decarboxylase in a Patient with Congenital Erythropoietic Porphyria and in His Family

Clinical Chemistry and Laboratory Medicine

Volumn 35, Issue 1, 1997, Pages 35-40

  Freesemann, Anne G ^a   Doss, Manfred O ^a   Hofweber, Klaus ^b  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

^b Kinderkrankenhaus St Marien   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

COPROPORPHYRIN; ERYTHROCYTE ENZYME; PORPHYRIN; UROPORPHYRINOGEN DECARBOXYLASE; UROPORPHYRINOGEN III SYNTHASE;

ADOLESCENT; ARTICLE; CASE REPORT; CONGENITAL ERYTHROPOIETIC PORPHYRIA; ENZYME ACTIVITY; ENZYME DEFICIENCY; ERYTHROCYTE; FAMILY STUDY; FEMALE; HUMAN; MALE; PRIORITY JOURNAL; URINARY EXCRETION;

ADOLESCENT; FEMALE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MALE; PEDIGREE; PORPHYRIA, ERYTHROPOIETIC; UROPORPHYRINOGEN DECARBOXYLASE;

EID: 0031044925     PISSN: 14346621     EISSN: 14374331     Source Type: Journal    
DOI: 10.1515/cclm.1997.35.1.35     Document Type: Letter

References (12)

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