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Updated: Sep 9, 2025

10:32
Transcriptomic Analysis of Human Retinal Surgical Specimens Using jouRNAl
Published on: August 14, 2013
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RS1遺伝子のスプライスサイト変異c.53-1G>Aに関連した網膜脱落:症例報告と文献のレビュー
Jia Meng1,2, Shanjun Cai1,2, Gang Su2,3
1Department of Ophthalmology, Affiliated Hospital of Zunyi Medical University, Guizhou Province, China.
SAGE open medical case reports
|September 2, 2025
まとめ
RS1遺伝子変異によって引き起こされるX関連網膜分裂は,さまざまな目の表型で表れます. この網膜疾患の診断には 遺伝子検査が不可欠です 特に症状が異なる場合です
科学分野:
- 眼科について
- 遺伝学
- 分子生物学
背景:
- RS1遺伝子によってコードされるレチノシシンタンパク質は,主に網膜で発現する.
- RS1遺伝子変異は,X関連網膜分裂の既知の原因であり,網膜の穴と層の分離によって特徴づけられる状態です.
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