一个新的有害的MYO15A基因突变导致非综合征性听力损失
Mostafa Neissi1, Adnan Issa Al-Badran2, Javad Mohammadi-Asl3
1Department of Genetics, Khuzestan Science and Research Branch, Islamic Azad University, Ahvaz, Iran. Department of Genetics, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran.
Iranian journal of otorhinolaryngology
|January 23, 2024
概括
在MYO15A基因的新型突变,MYO15A-p.Lys3303Thr,被确定为非综合征性听力损失 (NSHL) 的原因. 这一发现有助于为遗传性听力损失患者提供遗传咨询.
科学领域:
- 遗传学 是一个遗传学.
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
- 分子生物学分子生物学
背景情况:
- 听力损失 (HL) 是全球普遍存在的感官神经缺陷.
- 遗传因素是遗传HL的重要贡献者.
- 非综合征性听力损失 (NSHL) 没有其他相关的医疗条件.
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