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(Q24561674)

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Human adenine phosphoribosyltransferase. Identification of allelic mutations at the nucleotide level as a cause of complete deficiency of the enzyme

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Human adenine phosphoribosyltransferase. Identification of allelic mutations at the nucleotide level as a cause of complete deficiency of the enzyme (English)
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Y Hidaka
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T D Palella
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T E O'Toole
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S A Tarlé
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W N Kelley
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November 1987
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80
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5
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1409-15
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