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Research Article
A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.

Authors

    Citation

    Petersen CE, Scottolini AG, Cody LR, et al
    A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.
    Journal of Medical Genetics 1994;31:355-359.

    Publication history

    • First published May 1, 1994.
    Online issue publication 
    April 27, 2016

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