Publication | Closed Access
A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy
89
Citations
23
References
1999
Year
OphthalmologyCorneal DystrophyHelix Termination MotifMolecular BiologyMolecular GeneticsOcular PathologyUs FamilyMedicineKeratin K12
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