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An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb

Nathalie Brison1, Philippe Debeer, Sebastian Fantini

  • 1Laboratory of Skeletal Development and Joint Disorders, University of Leuven, Herestraat 49, O&N1 Box 813, 3000 Leuven, Belgium.

Human Molecular Genetics
|March 1, 2012
PubMed

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