Clinical haemochromatosis in HFE mutation carriers.

Timothy Cox, Jacques Rochette, Clara Camaschella, Ann Walker, Kathryn Robson

Research output: Contribution to journalArticle

33 Citations (Scopus)
Original languageEnglish
JournalLancet
Volume360
Issue number9330
Publication statusPublished - Aug 3 2002

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Cox, T., Rochette, J., Camaschella, C., Walker, A., & Robson, K. (2002). Clinical haemochromatosis in HFE mutation carriers. Lancet, 360(9330).

Clinical haemochromatosis in HFE mutation carriers. / Cox, Timothy; Rochette, Jacques; Camaschella, Clara; Walker, Ann; Robson, Kathryn.

In: Lancet, Vol. 360, No. 9330, 03.08.2002.

Research output: Contribution to journalArticle

Cox, T, Rochette, J, Camaschella, C, Walker, A & Robson, K 2002, 'Clinical haemochromatosis in HFE mutation carriers.', Lancet, vol. 360, no. 9330.
Cox T, Rochette J, Camaschella C, Walker A, Robson K. Clinical haemochromatosis in HFE mutation carriers. Lancet. 2002 Aug 3;360(9330).
Cox, Timothy ; Rochette, Jacques ; Camaschella, Clara ; Walker, Ann ; Robson, Kathryn. / Clinical haemochromatosis in HFE mutation carriers. In: Lancet. 2002 ; Vol. 360, No. 9330.
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