Tomokazu Takeuchi

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

Autosomal dominant familial exudative vitreoretinopathy in two Japanese families with<i>FZD4</i>mutations (H69Y and C181R)

Satoshi Omoto, Takaaki Hayashi, Kenji Kitahara et al. · Ophthalmic Genetics · 2004 · 42 citations

A Novel Haplotype with the R345W Mutation in the<i>EFEMP1</i>Gene Associated with Autosomal Dominant Drusen in a Japanese Family

Tomokazu Takeuchi, Takaaki Hayashi, Matthew Bedell et al. · Investigative Ophthalmology & Visual Science · 2010 · 39 citations · Full text

&lt;i&gt;CYP4V2&lt;/i&gt; Mutations in Two Japanese Patients with Bietti’s Crystalline Dystrophy

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