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ejhg.2015.169
ejhg.2015.169
https://scigraph.springernature.com/pub.10.1038/ejhg.2015.169
Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences.
P2888
Q37058489-65E87EDE-FC07-4107-8955-64A407DD576B
P2888
ejhg.2015.169
https://scigraph.springernature.com/pub.10.1038/ejhg.2015.169