Lattice Corneal Dystrophy Type III in Patients with a Homozygous L527R Mutation in the TGFBI Gene

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CLINICAL FEATURES OF JAPANESE LEBER'S HEREDITARY OPTIC NEUROPATHY WITH 11778 MUTATION OF MITOCHONDRIAL DNA
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Macular Nerve Fibers Temporal to Fovea May Have a Greater Potential to Recover Function in Patients With Leber's Hereditary Optic Neuropathy
Mitochondrial DNA Mutations with Leber's Hereditary Optic Neuropathy in Japanese Patients with Open-Angle Glaucoma
Lattice Corneal Dystrophy Type III in Patients with a Homozygous L527R Mutation in the TGFBI Gene
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