A Novel Mutation in The LHX3 Gene is Responsible for Combined Pituitary Hormone Deficiency, Hearing Impairment, and Vertebral Malformations

  • Kriström, Berit
  • Zdunek, Anna-Maija
  • Rydh, Anders
  • Jonsson, Håkan
  • Sehlin, Petra
  • Escher, Stefan A.

The following abstracts from The Journal of Clinical Endocrinology & Metabolism have been selected by the editors of Molecular Endocrinology as being particularly relevant to readers interested in translational science.

Molecular Endocrinology 23(2):p 277, February 2009.
Copyright © 2009 by The Endocrine Society