Multicentric carpotarsal osteolysis syndrome is caused by only a few domain-specific mutations inMAFB, a negative regulator of RANKL-induced osteoclastogenesis

Author:

Mumm Steven12,Huskey Margaret1,Duan Shenghui1,Wenkert Deborah2,Madson Katherine L.2,Gottesman Gary S.2,Nenninger Angela R.2,Laxer Ronald M.3,McAlister William H.4,Whyte Michael P.12

Affiliation:

1. Division of Bone and Mineral Diseases; Washington University School of Medicine at Barnes-Jewish Hospital; St. Louis Missouri

2. Center for Metabolic Bone Disease and Molecular Research; Shriners Hospital for Children; St. Louis Missouri

3. Division of Rheumatology, Departments of Pediatrics and Medicine; The Hospital for Sick Children and the University of Toronto; Toronto Canada

4. Department of Pediatric Radiology; Mallinckrodt Institute of Radiology at St. Louis Children's Hospital, Washington University School of Medicine; St. Louis Missouri

Funder

National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health

Shriners Hospitals for Children

The Clark and Mildred Cox Inherited Metabolic Bone Disease Research Fund

The Hypophosphatasia Research Fund

The Barnes-Jewish Hospital Foundation

The Frederick S. Upton Foundation

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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