Defective trafficking and localization of mutated transferrin receptor 2: implications for type 3 hereditary hemochromatosis. (Q34655528)

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Defective trafficking and localization of mutated transferrin receptor 2: implications for type 3 hereditary hemochromatosis.
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    Defective trafficking and localization of mutated transferrin receptor 2: implications for type 3 hereditary hemochromatosis (English)

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