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A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.
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    Petersen CE, Scottolini AG, Cody LR, et al
    A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.

    Publication history

    • First published May 1, 1994.
    Online issue publication 
    May 01, 1994

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