HYPOPARATHYROIDISM, DEAFNESS, AND RENAL DYSPLASIA

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Copy For Citation

CIVAN N., EREM C., COSKUN H., KOCAK M., Nuhoglu I., ERSOZ H. O.

ACTA ENDOCRINOLOGICA-BUCHAREST, vol.10, no.4, pp.687-692, 2014 (SCI-Expanded)

• Publication Type: Article / Article
• Volume: 10 Issue: 4
• Publication Date: 2014
• Doi Number: 10.4183/aeb.2014.687
• Journal Name: ACTA ENDOCRINOLOGICA-BUCHAREST
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
• Page Numbers: pp.687-692
• Karadeniz Technical University Affiliated: Yes

Abstract

Background. HDR syndrome is an autosomal dominant disorder characterized by hypoparathyroidism, sensorineural deafness, and renal dysplasia caused by mutation of the GATA3 gene.