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EJHG.2015.169
EJHG.2015.169
http://dx.doi.org/10.1038/EJHG.2015.169
Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences.
P356
Q37058489-2B104704-2A1C-46E0-846B-6FF40CFB8A8D
P356
EJHG.2015.169
http://dx.doi.org/10.1038/EJHG.2015.169