ORA - Oxford University Research Archive

1 - 5 of 5

1

Journal article

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

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

2

Journal article

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

Poulton, J, Macaulay, V, Livesey, K, et al.
2001-10-05

3

Journal article

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

Marston, S, Copeland, O, Jacques, A, et al.
2009-07-05

4

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

5

Journal article

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

Roetto, A, Merryweather-Clarke, AT, Daraio, F, et al.
2002-07-05

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