Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance.
(Investigative ophthalmology & visual science 2019)
High-Resolution Retinal Imaging Reveals Preserved Cone Photoreceptor Density and Choroidal Thickness in Female Carriers of Choroideremia.
(Ophthalmic surgery, lasers & imaging retina 2019)
Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohort.
(Molecular vision 2019)
Works (4件)：
新規ホメオボックス遺伝子(RlNX)の発現
1999 - 2001
Expression of a Novel Homeobox gene 'RlNX'
1999 - 2001
第2異常の分子メカニズム
1998 - 2001
Molecular Basis of Deutan Color Vision Defects
1998 - 2001
