Genetic irony beyond haemochromatosis: Clinical effects of HLA-H mutations

Lancet

Volumn 349, Issue 9048, 1997, Pages 296-297

  Beutler, E ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HLA ANTIGEN;

AMINO ACID SUBSTITUTION; GENE FREQUENCY; GENE MUTATION; HEMOCHROMATOSIS; HETEROZYGOTE; HISTOCOMPATIBILITY GENE; HUMAN; IMMUNOGENETICS; IRON METABOLISM; NUCLEIC ACID BASE SUBSTITUTION; PORPHYRIA CUTANEA TARDA; PRIORITY JOURNAL; SHORT SURVEY;

EID: 0031037009     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(97)22005-2     Document Type: Note

References (7)

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2. JN Feder A Gnirke W Thomas A novel MHC class I-like gene is mutated in patients with hereditary haemachromatosis Nat Genet 13 1996 399 408
3. E Beutler T Gelbart C West Mutation analysis in hereditary hemochromatosis Blood Cells Mol Dis 22 1996 187 194
4. L Calandro T Thorsen L Barcellos J Griggs D Baer GF Sensabaugh Mutation analysis in hereditary hemochromatosis Blood Cells Mol Dis 22 1996 194A 194B
5. EC Jazwinska LM Cullen F Busfield Haemochromatosis and HLA-H Nat Genet 14 1996 249 251
6. AM Jouanolle G Gandon P Jezequel Haemochromatosis and HLA-H Nat Genet 14 1996 251 252
7. ZJ Bulaj LM Griffen LB Jorde CQ Edwards JP Kushner Clinical and biochemical abnormalities in people heterozygous for hemochromatosis N Engl J Med 335 1996 1799 1805