P274: A case of IPEX syndrome caused by a novel mutation in FOXP3 gene, and exhibited abnormal osseous findings

• Duha Hejla,
• Cornelius Boerkoel, III

Affiliations

Duha Hejla

Department of Endocrinology, University of British Columbia and BC Children’s Hospital, Vancouver, BC, Canada

Cornelius Boerkoel, III

Provincial Medical Genetics Program, BC Women’s Hospital, Vancouver, BC, Canada, Department of Medical Genetics, University of British Columbia