Epidemic pathogenic selection: an explanation for hereditary hemochromatosis? (Q33961191)

30 July 2017

title

Epidemic pathogenic selection: an explanation for hereditary hemochromatosis? (English)

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30 July 2017

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Sharon Moalem

1

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30 July 2017

Maire E Percy

series ordinal

2

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30 July 2017

Theo P A Kruck

series ordinal

3

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30 July 2017

Richard R Gelbart

series ordinal

4

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30 July 2017

publication date

1 September 2002

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30 July 2017

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30 July 2017

volume

59

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30 July 2017

issue

3

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30 July 2017

page(s)

325-329

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Tay-Sachs disease carrier screening: a model for prevention of genetic disease

30 July 2017

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Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands

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Hemochromatosis: a genetic defect in iron metabolism

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Transferrin receptor is negatively modulated by the hemochromatosis protein HFE: implications for cellular iron homeostasis

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The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression

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Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis

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Prevalence of hereditary hemochromatosis in a Massachusetts corporation: is Celtic origin a risk factor?

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Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes

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7 January 2021

Celtic origin of the C282Y mutation of hemochromatosis

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Salmonellosis: host immune responses and bacterial virulence determinants.

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Salmonella typhi uses CFTR to enter intestinal epithelial cells.

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Soaring costs in defence

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7 January 2021

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Identifiers

DOI

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30 July 2017

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