|corneas, ciliary bodies, retinas and trabecular meshwork
|Mutation in MIR184 is a rare cause of KC alone and may be more relevant to cases of KC associated with other ocular abnormalities. The increased expression of miR-184 versus miR-205 in normal cornea samples implies a possible role of miR184 in cornea development and/or corneal diseases.
|Screening of the Seed Region of MIR184 in Keratoconus Patients from Saudi Arabia.
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