Primary hyperoxaluria type I due to a point mutation of T to C in the coding region of the serine:pyruvate aminotransferase gene (Q28279809)

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Primary hyperoxaluria type I due to a point mutation of T to C in the coding region of the serine:pyruvate aminotransferase gene
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    Primary hyperoxaluria type I due to a point mutation of T to C in the coding region of the serine:pyruvate aminotransferase gene (English)
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    K Nishiyama
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    T Funai
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    R Katafuchi
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    F Hattori
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    K Onoyama
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    A Ichiyama
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    15 May 1991
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    176
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    3
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    1093-9
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