在RDH8中的一个拼接变体与自体逆向Stargardt斑点变症有关
Stefania Zampatti1, Cristina Peconi1, Giulia Calvino1
1Genomic Medicine Laboratory UILDM, IRCCS Santa Lucia Foundation, 00179 Rome, Italy.
Genes
|August 26, 2023
概括
研究人员发现了一种新的遗传病因,导致Stargardt黄斑发育不良,这是一种罕见的眼睛疾病. 在一家意大利家庭中发现了RDH8基因的突变,标志着该类型的第一个报告病例.
科学领域:
- 眼科医生 眼科 眼科
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
背景情况:
- 斯塔格特斑点缩症 (Stargardt macular dystrophy,简称SMD) 是一种遗传性视网膜疾病,通常缺乏已知的遗传原因.
- 识别致病基因对于理解疾病机制和开发疗法至关重要.
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