A mutation in the SLC11A3 gene is associated with autosomal dominant hemochromatosis

Authors :: Njajou, O.T.
Vaessen, N.
Joosse, M.
Berghuis, B.
van Dongen, J.
Breuning, M.
Snijders, P.L.
Rutten, W.P.
Sandkuijl, L.
Oostra, B.A.
van Duijn, C.M.
Heutink, P.
Source :: American Journal of Human Genetics. Oct, 2001, Vol. 69 Issue 4, 626
Publication Year :: 2001

Subjects :: Human genetics -- Research
Hemochromatosis -- Genetic aspects
Genetic disorders -- Research
Biological sciences

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