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    Juvenile Paget’s disease with compound heterozygous mutations in TNFRSF11B presenting with recurrent clavicular fractures and a mild skeletal phenotype

    Juvenile Paget’s disease with compound heterozygous mutations in TNFRSF11B presenting with recurrent clavicular fractures and a mild skeletal phenotype by Naot, Dorit, Wilson, Louise C., Allgrove, Jeremy, Adviento, Eleanor, Piec, Isabelle, Musson, David S., Cundy, Tim, Calder, Alistair D.

    Published in Bone (New York, N.Y.)
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