Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High Myopia

Satoshi KatagiriDivision of Molecular and Cellular Biology, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan, ;Department of Ophthalmology, The Jikei University School of Medicine, Tokyo, Japan, and

Takaaki HayashiDepartment of Ophthalmology, The Jikei University School of Medicine, Tokyo, Japan, and Correspondence[email protected]

Kazutoshi YoshitakeLaboratory of DNA Data Analysis, National Institute of Genetics, Shizuoka, Japan

Masakazu AkahoriDivision of Molecular and Cellular Biology, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan,

Kazuho IkeoLaboratory of DNA Data Analysis, National Institute of Genetics, Shizuoka, Japan

Tamaki GekkaDepartment of Ophthalmology, The Jikei University School of Medicine, Tokyo, Japan, and

Hiroshi TsuneokaDepartment of Ophthalmology, The Jikei University School of Medicine, Tokyo, Japan, and

Takeshi IwataDivision of Molecular and Cellular Biology, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan,

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Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High Myopia

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Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High Myopia

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