Associated Papers
Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome.
Wang L et al.
Chinese Medical Journal, 2017
GATA3 abnormalities in six patients with HDR syndrome.
Fukami M et al.
Endocrine Journal, 2011
[Evaluation of deaf-mute patients with sensitive deafness gene screening in Shandong province].
Ji YB et al.
Zhonghua Yi Xue Za Zhi, 2009
A novel mutation in the GATA3 gene in a family with HDR syndrome (Hypoparathyroidism, sensorineural Deafness and Renal anomaly syndrome).
Adachi M et al.
Journal of Pediatric Endocrinology & Metabolism : Jpem, 2006
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