Satoshi Goto‐Omoto

Novel NR2E3 Mutations (R104Q, R334G) Associated with a Mild Form of Enhanced S-Cone Syndrome Demonstrate Compound Heterozygosity

Takaaki Hayashi, Tamaki Gekka, Satoshi Goto‐Omoto et al. · Ophthalmology · 2005 · 46 citations

Mild Form, Mendelian Disorder, Genetic Disorder +9

A Novel Homozygous GRK1 Mutation (P391H) in 2 Siblings with Oguchi Disease with Markedly Reduced Cone Responses

Takaaki Hayashi, Tamaki Gekka, Tomokazu Takeuchi et al. · Ophthalmology · 2006 · 43 citations

Oguchi Disease, Mendelian Disorder, Genetic Disorder +6

<i>CYP4V2</i> Mutations in Two Japanese Patients with Bietti’s Crystalline Dystrophy

Tamaki Gekka, Takaaki Hayashi, Tomokazu Takeuchi et al. · Ophthalmic Research · 2005 · 35 citations

Compound heterozygous <i>CNGA3</i> mutations (R436W, L633P) in a Japanese patient with congenital achromatopsia

Satoshi Goto‐Omoto, Takaaki Hayashi, Tamaki Gekka et al. · Visual Neuroscience · 2006 · 32 citations

Compound heterozygous <i>RDH5</i> mutations in familial fleck retina with night blindness

Takaaki Hayashi, Satoshi Goto‐Omoto, Tomokazu Takeuchi et al. · Acta Ophthalmologica Scandinavica · 2005 · 16 citations