Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.

Cellular and molecular biology (Noisy-le-Grand, France)

Volumn 48, Issue 1, 2002, Pages 49-55

  Gross, U ^a   Puy, H ^a   Kuhnel A ^a   Meissauer, U ^a   Deybach, J C ^a   Jacob, K ^a   Martasek, P ^a   Nordmann, Y ^a   Doss, M O ^a  

^a UNIVERSITY HOSPITAL MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

COPROPORPHYRIN; COPROPORPHYRIN III; COPROPORPHYRINOGEN OXIDASE;

ADULT; CASE REPORT; ENZYMOLOGY; FAMILY HEALTH; FEMALE; GENETICS; HEPATIC PORPHYRIA; HETEROZYGOTE; HUMAN; NUCLEOTIDE SEQUENCE; PEDIGREE; PORPHYRIA CUTANEA TARDA; REVIEW;

ADULT; COPROPORPHYRINOGEN OXIDASE; COPROPORPHYRINS; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; HETEROZYGOTE; HUMANS; PEDIGREE; PORPHYRIA CUTANEA TARDA; PORPHYRIAS, HEPATIC;

EID: 0036483509     PISSN: 01455680     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (31)