A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen Syndrome (Q36045072)

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A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen Syndrome
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    A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen Syndrome (English)
    Jennifer J Johnston
    Julie Sapp
    Molly Crenshaw
    NiCole A Finch
    Virginia P Sybert
    12 August 2015
    465-474

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