المؤلفون: Kuniyoshi K; Department of Ophthalmology, Kinki University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama City, Osaka, 589-8511, Japan, kuniyoshi-kazuki@umin.net., Sakuramoto H, Yoshitake K, Ikeo K, Furuno M, Tsunoda K, Kusaka S, Shimomura Y, Iwata T

المصدر: Documenta ophthalmologica. Advances in ophthalmology [Doc Ophthalmol] 2015 Aug; Vol. 131 (1), pp. 71-9. Date of Electronic Publication: 2015 Apr 01.

نوع المنشور: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Kluwer Country of Publication: Netherlands NLM ID: 0370667 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-2622 (Electronic) Linking ISSN: 00124486 NLM ISO Abbreviation: Doc Ophthalmol Subsets: MEDLINE

مواضيع طبية MeSH: Electroretinography* , Mutation*, Asian People/*genetics , Cyclic Nucleotide Phosphodiesterases, Type 6/*genetics , Retinal Rod Photoreceptor Cells/*physiology , Retinitis Pigmentosa/*genetics, Adult ; Aged ; Aged, 80 and over ; Exome/genetics ; Female ; Heterozygote ; High-Throughput Nucleotide Sequencing ; Humans ; Japan ; Male ; Middle Aged ; Pedigree ; Photic Stimulation ; Retinitis Pigmentosa/physiopathology ; Siblings ; Vision Disorders/physiopathology ; Visual Acuity/physiology ; Visual Field Tests ; Visual Fields/physiology