首页> Molecular genetics and genomics: MGG> Mutational investigation of 17 causative genes in a cohort of 113 families with nonsyndromic early-onset high myopia in northwestern China

Mutational investigation of 17 causative genes in a cohort of 113 families with nonsyndromic early-onset high myopia in northwestern China

导出原文传递

翻译打印收藏纠错

第一作者： Ye, Min

作者： Ye, Min ^[1] ; Ma, Ya ^[2] ; Qin, Yi-Xuan ^[3] ; Cai, Bo ; Ma, Li-mei ; Ma, Zhen ; Liu, Yang ; Jin, Zi-Bing ; Zhuang, Wen-Juan

作者单位： Capital Med Univ ^[1] Ningxia Med Univ ^[2] North Minzu Univ ^[3]

关键词 Whole-exome sequencing Early-onset high myopia Gene Variant PATHOLOGICAL MYOPIA EPIDEMIOLOGY GENETICS NDUFAF7 VARIANT ZNF644 IDENTIFICATION PATHWAY SLC39A5 LRPAP1

发布时间 2023-09-09

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交

浏览0

Molecular genetics and genomics

2023年298卷3期

669-682页

相似文献

中文期刊
外文期刊
学位论文
会议论文

浏览0

点击下载本期目录封面

Molecular genetics and genomics

2023年298卷3期

669-682页

检索历史清除

Mutational investigation of 17 causative genes in a cohort of 113 families with nonsyndromic early-onset high myopia in northwestern China

Molecular genetics and genomics

相似文献

同项目论文

Molecular genetics and genomics

相关期刊

参考文献：
指定格式：	NoteExpress EndNote RefWorks NoteFirst

检索历史 清除

Mutational investigation of 17 causative genes in a cohort of 113 families with nonsyndromic early-onset high myopia in northwestern China

Molecular genetics and genomics

相似文献

同项目论文

Molecular genetics and genomics

相关期刊

检索历史清除