Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosis (Q33679433)

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Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosis
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    Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosis (English)
    1 September 1997

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