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

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

J. Gécz | M. Bitner-Glindzicz | J. Tolmie | B. Harding | I. Grigorieva | H. Van Esch | B. Gilbert-Dussardier | P. Clayton | C. Mache | A. Ong | M. Nesbit | R. Thakker | G. Hendy | F. Lalloo | A. Hackett | J. Weill | S. Smithson | P. Christie | Z. Mughal | N. Shaw | Asif Ali | E. Guillén-Navarro | E. Blind | C. Rinat | P. Christin | C. Bloch | I. Halac | S. Ahmed | S. Ahmed