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Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome
Authors:Nesbit M Andrew  Bowl Michael R  Harding Brian  Ali Asif  Ayala Alejandro  Crowe Carol  Dobbie Angus  Hampson Geeta  Holdaway Ian  Levine Michael A  McWilliams Robert  Rigden Susan  Sampson Julian  Williams Andrew J  Thakker Rajesh V
Institution:Nuffield Department of Medicine, University of Oxford, Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford OX3 7LJ, United Kingdom.
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