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Academic Press

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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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C677T gene mutation in methylenetetrahydrofolate reductase as a risk factor for cardiac allograft vasculopathy

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Transplantation Proceedings, Vol. 31, Iss. 1, 1999-02 ,pp. : 99-99

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Identification of a Novel Pancreatitis-Associated Missense Mutation, R116C, in the Human Cationic Trypsinogen Gene (PRSS1)

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Functional expression of the TrkC gene, encoding a high affinity receptor for NT-3, in antigen-specific T helper type 2 (Th2) cells

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