A kerato-epithelin (betaig-h3) mutation in lattice corneal dystrophy type IIIA.
Yamamoto S, Okada M, Tsujikawa M, Shimomura Y, Nishida K, Inoue Y, Watanabe H, Maeda N, Kurahashi H, Kinoshita S, Nakamura Y, Tano Y.
Yamamoto S, et al. Among authors: tsujikawa m.
Am J Hum Genet. 1998 Mar;62(3):719-22. doi: 10.1086/301765.
Am J Hum Genet. 1998.
PMID: 9497262
Free PMC article.
No abstract available.