Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects
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| Description | scientific article |
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author: Veronica van Heyningen Carl A Anderson Martin S. Taylor Alain Verloes Matthew Hurles David FitzPatrick Andrew Oliver Mungo Wilkie |
| Publication date | February 6, 2014 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |