Ali, A. et al. (2007) Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor. Human Molecular Genetics, 16, pp. 265-275.
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| Item Type: | Articles |
|---|---|
| Status: | Published |
| Refereed: | Yes |
| Glasgow Author(s) Enlighten ID: | Ahmed, Dr Syed and Ahmed, Professor Syed Faisal |
| Authors: | Ali, A., Christie, P., Grigorieva, I., Harding, B., Van Esch, H., Ahmed, S., Ahmed, S., Bitner-Glindzicz, M., Blind, E., Bloch, C., Christin, P., Clayton, P., Gecz, J., Gilbert-Dussardier, B., Guillen-Navarro, E., Hackett, A., Halac, I., Hendy, G., Lalloo, F., and Mache, C. |
| College/School: | College of Medical Veterinary and Life Sciences |
| Journal Name: | Human Molecular Genetics |
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