Mutations of the hereditary hemochromatosis candidate gene HLA-H in porphyria cutanea tarda [6]

New England Journal of Medicine

Volumn 336, Issue 18, 1997, Pages 1327-1328

  Santos, M ^a   Clevers, H C ^a   Marx, J J M ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

HLA H ANTIGEN; IRON; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1; UNCLASSIFIED DRUG; UROPORPHYRIN; UROPORPHYRINOGEN DECARBOXYLASE;

ALLELE; CLINICAL ARTICLE; CONTROLLED STUDY; ENZYME DEFECT; GENE MUTATION; HEMOCHROMATOSIS; HETEROZYGOTE; HLA SYSTEM; HUMAN; IRON METABOLISM; LETTER; PHLEBOTOMY; POLYMERASE CHAIN REACTION; PORPHYRIA CUTANEA TARDA; PRIORITY JOURNAL;

GENES, MHC CLASS I; HEMOCHROMATOSIS; HISTOCOMPATIBILITY ANTIGENS CLASS I; HLA ANTIGENS; HUMANS; MEMBRANE PROTEINS; POINT MUTATION; PORPHYRIA CUTANEA TARDA;

EID: 0030956314     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJM199705013361817     Document Type: Letter

References (5)