Haemochromatosis gene C282Y homozygotes in an elderly male population

Lancet

Volumn 354, Issue 9174, 1999, Pages 221-222

  Willis, Gavin ^a   Wimperis, Jennie Z ^a   Smith, Katy C ^a   Fellows, Ian W ^a   Jennings, Barbara A ^a  

^a NORFOLK AND NORWICH HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AGED; ARTICLE; CASE REPORT; GENE MUTATION; HEMOCHROMATOSIS; HOMOZYGOTE; HUMAN; HUMAN CELL; MALE; NORMAL HUMAN; PRIORITY JOURNAL;

EID: 0033578246     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(99)02195-9     Document Type: Article

References (5)

1. McDonnell S.M., Phatak P.D., Felitti V., Hover A., McLaren G.D. Screening for hemochromatosis in primary care settings. Ann Intern Med. 129:1998;962-970.
2. Feder J.N., Gnirke A., Thomas W.et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nature Genet. 13:1996;399-408.
3. Willis G., Wimperis J.Z., Lonsdale R., Jennings B.A. Haemochromatosis gene mutation in hepatocellular cancer. Lancet. 350:1997;565-566.
4. Willis G., Wimperis J.Z., Lonsdale R., Sampson M.J., Jennings B.A. Low-penetrance of HFE mutation in an English population. Blood. 92:1998;5506a.
5. Niederau C., Fischer R., Purschel A., Stremmel W., Haussinger D., Strohmeyer G. Long-term survival in patients with hereditary hemochromatosis. Gastroenterology. 110:1996;1107-1119.