University of Oxford-ko ikertzaileekin lankidetzan egindako argitalpenak (1)

2007

  1. 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, Vol. 16, Núm. 3, pp. 265-275