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1598972
1598972
https://w3id.org/oc/corpus/br/1598972
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects
P3181
373dd3a23e7ba4ce52ab9853d7bb252f46c5a587
P3181
Q28306581-FBC4F4E0-F470-4815-AF7D-51FE9E2AD4B8
P3181
1598972
https://w3id.org/oc/corpus/br/1598972