Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects

Kathleen A. Williamson, Joe Rainger, James Floyd, Morad Ansari, Alison Meynert, Kishan V. Aldridge, Jacqueline K. Rainger, Carl A. Anderson, Anthony T. Moore, Matthew E. Hurles,

The American Journal of Human Genetics · 2014 · 109 citations · 30 references

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