Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects
Titel:
Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects
Auteur:
Williamson, Kathleen A. Rainger, Joe Floyd, James A.B. Ansari, Morad Meynert, Alison Aldridge, Kishan V. Rainger, Jacqueline K. Anderson, Carl A. Moore, Anthony T. Hurles, Matthew E. Clarke, Angus van Heyningen, Veronica Verloes, Alain Taylor, Martin S. Wilkie, Andrew O.M. FitzPatrick, David R.