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A New Mutation (Leu569Arg) Within Exon 13 of the ßig-h3 Gene Causes Lattice Corneal Dystrophy Type I
A New Mutation (Leu569Arg) Within Exon 13 of the ßig-h3 Gene Causes Lattice Corneal Dystrophy Type I
2003
J.F. Warren
R.L. Abbott
J.B. Crawford
William H. Spencer
T.P. Margolis
Keywords:
Lattice corneal dystrophy
Diabetes mellitus
Genetics
Exon
Anatomy
Gene
New mutation
Biology
Correction
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