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A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann’s corneal dystrophy
  1. Correspondence to: M K Yoon Francis I Proctor Foundation, 95 Kirkham Street, San Francisco, CA 94143, USA; myoonitsa.ucsf.edu
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Yoon MK, Warren JF, Holsclaw DS, et al
A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann’s corneal dystrophy

Publication history

  • Accepted October 4, 2003
  • First published May 17, 2004.
Online issue publication 
March 22, 2016

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