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A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy

✍ Scribed by Carrie M. Coleman; Sadeer Hannush; Seana P. Covello; Frances J.D. Smith; Jouni Uitto; W.H.Irwin McLean

No coin nor oath required. For personal study only.

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