A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.
Njajou OT; Vaessen N; Joosse M; Berghuis B; van Dongen JW; Breuning MH; Snijders PJ; Rutten WP; Sandkuijl LA; Oostra BA; van Duijn CM; Heutink P; Nature Genetics, 2001, vol. 28, issue 3, p 213, ISSN 10614036. ISBN 10614036.

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