Novel Gross Deletion Mutations in <i>NTRK1</i> Gene Associated With Congenital Insensitivity to Pain With Anhidrosis.

导出 LinkOut

翻译打印收藏纠错

作者： Lulu,Li ^[1] ; Chao,Jia ^[2] ; Yue,Tang ^[1] ; Yuanyuan,Kong ^[1] ; Yaofang,Xia ^[2] ; Li,Ma ^[2]

作者单位： Department of Newborn Screening Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, China. ^[1] Department of Neonatology, Hebei Provincial Children's Hospital, Shijiazhuang, China. ^[2]

关键词 CIPA Chinese families HSAN NTRK1 mutations whole exome sequencing

DOI 10.3389/fped.2021.638190

PMID 33748046

发布时间 2021-03-23

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

Frontiers in pediatrics

2021年9卷

638190页

相似文献

中文期刊
外文期刊
学位论文
会议论文

检索历史清除

Novel Gross Deletion Mutations in <i>NTRK1</i> Gene Associated With Congenital Insensitivity to Pain With Anhidrosis.

Frontiers in pediatrics

相似文献

Frontiers in pediatrics

相关期刊

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

检索历史 清除

Novel Gross Deletion Mutations in <i>NTRK1</i> Gene Associated With Congenital Insensitivity to Pain With Anhidrosis.

Frontiers in pediatrics

相似文献

Frontiers in pediatrics

相关期刊

检索历史清除