A Novel De novo GATA?binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural

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INTRODUCTIONrnHypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome, also called Barakat syndrome, is an autosomal dominant genetic disease caused by haploinsufficiency of the GATA?binding protein 3 (GATA3) gene located on the 10p15 chromosome.
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