Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: Insight into mechanisms of DNA binding by the GATA3 transcription factor

1. Ali, A.
2. Christie, P.T.
3. Grigorieva, I.V.
4. Harding, B.
5. Van Esch, H.
6. Ahmed, S.F.
7. Bitner-Glindzicz, M.
8. Blind, E.
9. Bloch, C.
10. Christin, P.
11. Clayton, P.
12. Gecz, J.
13. Gilbert-Dussardier, B.
14. Guillen-Navarro, E.
15. Hackett, A.
16. Halac, I.
17. Hendy, G.N.
18. Lalloo, F.
19. Mache, C.J.
20. Mughal, Z.
21. Ong, A.C.M.
22. Rinat, C.
23. Shaw, N.
24. Smithson, S.F.
25. Tolmie, J.
26. Weill, J.
27. Nesbit, M.A.
28. Thakker, R.V.
29. Mostrar todos os autores +