A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 ( PIEZO2) induced tracheobronchomalacia

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作者 Wu Juan ^[1] Zhong Lin ^[2] Chen Ting ^[2] Qiu Li ^[2] Li Yi-Fei ^[1] 学术成果认领

作者单位 Key Laboratory of Birth Defects and Related Diseases of Women and Children of MOE, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610041, China ^[1] Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610041, China ^[2]

栏目名称 Correspondence

DOI 10.1097/CM9.0000000000001500

发布时间 2025-02-25

基金项目

This research was supported by a grant from the Technology Project of Sichuan Province

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中华医学杂志英文版

2021年134卷10期

1254-1256页

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A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 ( PIEZO2) induced tracheobronchomalacia

A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 ( PIEZO2) induced tracheobronchomalacia

中华医学杂志英文版

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中华医学杂志英文版

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A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 ( PIEZO2) induced tracheobronchomalacia

A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 ( PIEZO2) induced tracheobronchomalacia

中华医学杂志英文版

相似文献

中华医学杂志英文版

相关期刊

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