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Rare Diseases Volume 1, 2013 - Issue 1
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Addendum

From an orphan disease to a generalized molecular mechanism

PTPN11 loss-of-function mutations in the pathogenesis of metachondromatosis

Wentian Yang Department of Orthopaedics and COBRE Center for Stem Cell Biology; Brown University Alpert Medical School and Rhode Island Hospital; Providence, RI USACorrespondence[email protected]
&
Benjamin G Neel Princess Margaret Cancer Center; University Health Network and Department of Medical Biophysics; University of Toronto; Toronto, ON Canada
Article: e26657 | Received 26 Aug 2013, Accepted 30 Sep 2013, Published online: 02 Oct 2013

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