Severe corneal dystrophy phenotype caused by homozygous R124H keratoepithelin mutations.

Masaki Okada(Foundation for Advancement of International Science), Y. Tano(The University of Osaka), Suguru Yamamoto(Niigata University), Hiroki Watanabe(The University of Osaka), Y Ishii(The University of Osaka), Yutaka Inoue(The University of Osaka), Y. Shimomura(The University of Osaka), Naoyuki Maeda(The University of Osaka)
PubMed
September 1, 1998
Cited by 86

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