Hereditary coproporphyria

Seminars in Liver Disease

Volumn 18, Issue 1, 1998, Pages 25-32

  Martásek, Pavel ^a  

^a UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

Author keywords

Coproporphyria; Coproporphyrinogen oxidase; Molecular pathology; Mutations

Indexed keywords

COPROPORPHYRINOGEN OXIDASE; PROTOPORPHYRINOGEN OXIDASE;

CLINICAL FEATURE; CONGENITAL ERYTHROPOIETIC PORPHYRIA; DNA DETERMINATION; EPILEPSY; FEVER; FLUORESCENCE; GASTROINTESTINAL SYMPTOM; GENE MUTATION; GENETIC CODE; GENETIC DISORDER; HUMAN; HYPERTENSION; LIVER DISEASE; PARALYSIS; PATIENT CARE; PRIORITY JOURNAL; REVIEW;

EID: 0031889894     PISSN: 02728087     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-1007137     Document Type: Review

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