Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.

The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder caused by mutations of the dual zinc finger transcription factor, GATA3. The C-terminal zinc finger (ZnF2) binds DNA, whereas the N-terminal finger (ZnF1) stabilizes this DNA binding and interacts...

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Bibliographic Details
Main Authors:	Nesbit, M, Bowl, MR, Harding, B, Ali, A, Ayala, A, Crowe, C, Dobbie, A, Hampson, G, Holdaway, I, Levine, M, McWilliams, R, Rigden, S, Sampson, J, Williams, A, Thakker, R
Format:	Journal article
Language:	English
Published:	2004

Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.

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