中华耳科学杂志（英文版）2025，Vol.20Issue(2)：67-71,5.DOI:10.26599/JOTO.2025.9540011
Case report of a novel GREB1L gene mutation in a patient with branchio-oto-renal syndrome
Case report of a novel GREB1L gene mutation in a patient with branchio-oto-renal syndrome
Sijing Chen 1Zixuan Yang 2Maoxin Wang 2Cuiping Zhong1
作者信息
- 1. The Second Clinical Medical School,Lanzhou University,Lanzhou,730030,China||Department of Otolaryngology-Head and Neck Surgery,the 940th Hospital of Joint Logistics Support Force of the Chinese People's Liberation Army,Lanzhou,730050,China
- 2. Department of Otolaryngology-Head and Neck Surgery,the 940th Hospital of Joint Logistics Support Force of the Chinese People's Liberation Army,Lanzhou,730050,China
- 折叠
摘要
关键词
Branchio-oto-renal syndrome/GREB1L/Hearing loss/Kidney agenesisKey words
Branchio-oto-renal syndrome/GREB1L/Hearing loss/Kidney agenesis引用本文复制引用
Sijing Chen,Zixuan Yang,Maoxin Wang,Cuiping Zhong..Case report of a novel GREB1L gene mutation in a patient with branchio-oto-renal syndrome[J].中华耳科学杂志（英文版）,2025,20(2):67-71,5.
