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Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation.
Jacek P Szaflik, Monika Ołdak, Radosław B Maksym, Anna Kamińska, Agnieszka Pollak, Monika Udziela, Rafał Płoski, Jerzy Szaflik
Mol Vis 2008; 14 1713-1718
ICID: 869745
IC™ Value: 12.33
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