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Research Article
A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans.

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    Citation

    Wilkes D, Rutland P, Pulleyn LJ, et al
    A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans.
    Journal of Medical Genetics 1996;33:744-748.

    Publication history

    • First published September 1, 1996.
    Online issue publication 
    April 27, 2016

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