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Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 → Cys mutation in the kerato-epithelin gene

✍ Scribed by Sanjoy K. Gupta; William G. Hodge; Karim F. Damji; Duane L. Guernsey; Paul E. Neumann

Book ID: 117020565
Publisher: Elsevier Science
Year: 1998
Tongue: English
Weight: 315 KB
Volume: 125
Category: Article
ISSN: 0002-9394
DOI: 10.1016/s0002-9394(99)80196-2

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