Search results - ORA - Oxford University Research Archive

1 - 10 of 10

1

Journal article

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4.

Roetto, A, Merryweather-Clarke, A, Daraio, F, et al.
2002-07-01

2

Journal article

Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.

Robson, K, Lehmann, D, Wimhurst, V, et al.
2004-04-01

3

Journal article

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.

Merryweather-Clarke, A, Cadet, E, Bomford, A, et al.
2003-09-01

4

Journal article

The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.

Livesey, K, Wimhurst, V, Carter, K, et al.
2004-01-01

5

Journal article

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4.

Roetto, A, Merryweather-Clarke, A, Daraio, F, et al.
2002-07-15

6

Journal article

A common mtDNA variant may be a susceptibility factor in 3 multifactorial diseases.

Poulton, J, Macaulay, V, Livesey, K, et al.
2001-10-01

7

Journal article

Pilot study of early diagnosis of hereditary haemochromatosis through systematic case finding in primary care.

Emery, J, Rose, P, Harcourt, J, et al.
2002-01-01

8

Journal article

Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency.

Marston, S, Copeland, O, Jacques, A, et al.
2009-07-01

9

Journal article

Hemochromatosis gene (HFE) mutations in South East Asia: a potential for iron overload.

Pointon, J, Viprakasit, V, Miles, K, et al.
2003-01-01

10

Journal article

A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis.

Cadet, E, Capron, D, Perez, A, et al.
2003-02-01

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