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S00417-017-3699-5
S00417-017-3699-5
http://dx.doi.org/10.1007/S00417-017-3699-5
Mutation analysis of TGFBI and KRT12 in a case of concomitant keratoconus and granular corneal dystrophy.
P356
Q38752233-A8C3436D-9314-4346-82F5-EE5B0F1E2FA6
P356
S00417-017-3699-5
http://dx.doi.org/10.1007/S00417-017-3699-5