Publication
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor
A. Ali, P. T. Christie, I. V. Grigorieva, B. Harding, H. Van Esch, S. F. Ahmed, M. Bitner-Glindzicz, E. Blind, C. Bloch, P. Christin, P. Clayton, J. Gecz, B. Gilbert-Dussardier, E. Guillen-Navarro, A. Hackett, I. Halac, G. N. Hendy, F. Lalloo, C. J. Mache, Z. Mughal, A. C.M. Ong, C. Rinat, N. Shaw, S. F. Smithson, J. Tolmie, J. Weill, M. A. Nesbit, R. V. Thakker
Human Molecular Genetics, December 2006, Oxford University Press (OUP)
DOI: 10.1093/hmg/ddl454