Novel molecular defects of the δ-aminolevulinate dehydratase gene in a patient with inherited acute hepatic porphyria

Hepatology

Volumn 31, Issue 3, 2000, Pages 704-708

  Akagi, Reiko ^a,b   Shimizu, Ryo ^a   Furuyama, Kazumichi ^b   Doss, Manfred O ^c   Sassa, Shigeru ^b  

^a OKAYAMA PREFECTURAL UNIVERSITY   (Japan)

^b ROCKEFELLER UNIVERSITY   (United States)

^c PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MESSENGER RNA; PORPHOBILINOGEN SYNTHASE;

ADULT; ALLELE; ANIMAL CELL; ARTICLE; CASE REPORT; CHO CELL; CONTROLLED STUDY; DNA DETERMINATION; ENZYME ACTIVITY; ENZYME DEFICIENCY; EPSTEIN BARR VIRUS; ERYTHROCYTE; GENE EXPRESSION; GENE MUTATION; HEPATIC PORPHYRIA; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL; MALE; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

EID: 0034005112     PISSN: 02709139     EISSN: None     Source Type: Journal    
DOI: 10.1002/hep.510310321     Document Type: Article

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