在PAX1基因中发生的一种新型切断突变会导致没有免疫缺陷的耳鼻椎综合征
Nagham M Elbagoury1, Asmaa F Abdel-Aleem2, Wessam E Sharaf-Eldin1
1Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
Journal of molecular neuroscience : MN
|November 4, 2023
概括
耳鼻椎综合征 (OTFCS) 是一种罕见的遗传疾病. 研究人员在一名埃及患者身上发现了一种新的PAX1基因突变,扩大了OTFCS2.2已知的地理范围.
科学领域:
- 遗传学和分子生物学
- 发展生物学 发展生物学
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
背景情况:
- 耳鼻椎综合征 (OTFCS) 是一种罕见的遗传疾病,具有自体逆向和主导遗传模式.
- 已知PAX1或EYA1基因的突变是OTFCS的已知原因.
- OTFCS2是一种与PAX1基因突变相关的特定亚型.
关键词:
面部形状障碍症 面部形状障碍症智力障碍 智力障碍是一种智力障碍.耳鼻椎综合征 (Otofaciocervical Syndrome) 是一种耳鼻椎综合征.一个PAX1基因.整个外基因组的测序.更多相关视频
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