文献
J-GLOBAL ID:201202281812913383
整理番号:12A1065641
錐体オプシンmRNAエクソン3の特異なハプロタイプは先天性色覚欠陥につながるその前駆体スプライシングに影響を与える
Unique haplotype in exon 3 of cone opsin mRNA affects splicing of its precursor, leading to congenital color vision defect
著者 (7件):
UEYAMA Hisao
(Dep. of Molecular Medical Biochemistry, Shiga Univ. of Medical Sci., Seta, Otsu 520-2192, JPN)
,
MURAKI-ODA Sanae
(Dep. of Ophthalmology, Shiga Univ. of Medical Sci., Seta, Otsu 520-2192, JPN)
,
YAMADE Shinichi
(Dep. of Ophthalmology, Shiga Univ. of Medical Sci., Seta, Otsu 520-2192, JPN)
,
TANABE Shoko
(Inst. of Vision Res., Atsuta-ku, Nagoya 456-0032, JPN)
,
YAMASHITA Takahiro
(Dep. of Biophysics, Graduate School of Sci., Kyoto Univ., Kyoto 606-8502, JPN)
,
SHICHIDA Yoshinori
(Dep. of Biophysics, Graduate School of Sci., Kyoto Univ., Kyoto 606-8502, JPN)
,
OGITA Hisakazu
(Dep. of Molecular Medical Biochemistry, Shiga Univ. of Medical Sci., Seta, Otsu 520-2192, JPN)
資料名:
Biochemical and Biophysical Research Communications
(Biochemical and Biophysical Research Communications)
巻:
424
号:
1
ページ:
152-157
発行年:
2012年07月20日
JST資料番号:
B0118A
ISSN:
0006-291X
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
オランダ (NLD)
言語:
英語 (EN)