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

Published in:

Human Molecular Genetics, 2007, v. 16, n. 3, p. 265

By:

• Ali, Asif;
• Christie, Paul T.;
• Grigorieva, Irina V.;
• Harding, Brian;
• Van Esch, Hilde;
• Ahmed, S. Faisal;
• Bitner-Glindzicz, Maria;
• Blind, Eberhard;
• Bloch, Catherine;
• Christin, Patricia;
• Clayton, Peter;
• Gecz, Jozef;
• Gilbert-Dussardier, Brigitte;
• Guillen-Navarro, Encarna;
• Hackett, Anna;
• Halac, Isil;
• Hendy, Geoffrey N.;
• Lalloo, Fiona;
• Mache, Christoph J.;
• Mughal, Zulf

Publication type:

Article