A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

Author:

Feder J.N.,Gnirke A.,Thomas W.,Tsuchihashi Z.,Ruddy D.A.,Basava A.,Dormishian F.,Domingo R.,Ellis M.C.,Fullan A.,Hinton L.M.,Jones N.L.,Kimmel B.E.,Kronmal G.S.,Lauer P.,Lee V.K.,Loeb D.B.,Mapa F.A.,McClelland E.,Meyer N.C.,Mintier G.A.,Moeller N.,Moore T.,Morikang E.,Prass C.E.,Quintana L.,Starnes S.M.,Schatzman R.C.,Brunke K.J.,Drayna D.T.,Risch N.J.,Bacon B.R.,Wolff R.K.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference76 articles.

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2. Edwards, C.Q. et al. Prevalence of hemochromatosis among 11,065 presumably healthy blood donors. N. Engl. J. Med. 318, 1355–1362 (1988).

3. McKusick, V.A. Mendelian inheritance in man (The Johns Hopkins University Press, Baltimore, 1994).

4. Bothwell, T.H., Charlton, R.W. & Motulski, A.G. in The metabolic and molecular bases of inherited disease (eds. Scriver, C.R., Beaudet, A.L., Sly, W.S. & Valle, D.) 2237–2269 (McGraw-Hill, New York, 1995).

5. Bacon, B.R. & Tavill, A.S., in Hepatology. A textbook of liver disease (eds. Zakim, D. & Boyer, T.D.) 1439–1472 (W.B. Saunders, Philadelphia, 1996).

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