Lack of clinical manifestation of hereditary haemochromatosis in South African patients with multiple sclerosis

Author:

Kotze Maritha J.,de Villiers J Nico P,Warnich Louise,Schmidt Stephen,Carr Jonathan,Mansvelt Erna,Fourie Elba,van Rensburg Susan J

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Biochemistry

Reference47 articles.

1. Aisen P (1994) Iron metabolism: an evolutionary perspective. In: Brock JH, Halliday JW, Pippard MJ, Powell LW (eds) Iron metabolism in health and disease, Saunders Co. Ltd. London. pp 1–30

2. Beutler E, Felitti VJ, Koziol JA, Ho NJ, Gelbart T (2002) Penetrance of 845G–> A (C282Y) HFE hereditary haemochromatosis mutation in the USA. Lancet 359:211–8

3. Day RS (1986) Variegate porphyria. Seminars in Dermatology 5:138–154

4. De Villiers JNP (2003). A multi-disciplinary approach towards elucidating the aetiology of multiple sclerosis. PhD thesis, University of Stellenbosch

5. De Villiers JNP, Kotze MJ (1999) Significance of linkage disequilibrium between mutation C282Y and a MseI polymorphism in population screening and DNA diagnosis of hemochromatosis. Blood Cells Molecules and Disease 15:250–252

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