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. Erakutsi egile guztiak +
Aldizkaria:
Human Molecular Genetics

ISSN: 0964-6906 1460-2083

Argitalpen urtea: 2007

Alea: 16

Zenbakia: 3

Orrialdeak: 265-275

Mota: Artikulua

DOI: 10.1093/HMG/DDL454 GOOGLE SCHOLAR

Garapen Iraunkorreko Helburuak