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A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 (PIEZO2) induced tracheobronchomalacia
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143733/ https://www.ncbi.nlm.nih.gov/pubmed/33928917 http://dx.doi.org/10.1097/CM9.0000000000001500 |
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author | Wu, Juan Zhong, Lin Chen, Ting Qiu, Li Li, Yi-Fei |
author_facet | Wu, Juan Zhong, Lin Chen, Ting Qiu, Li Li, Yi-Fei |
author_sort | Wu, Juan |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-8143733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-81437332021-05-26 A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 (PIEZO2) induced tracheobronchomalacia Wu, Juan Zhong, Lin Chen, Ting Qiu, Li Li, Yi-Fei Chin Med J (Engl) Correspondence Lippincott Williams & Wilkins 2021-05-20 2021-04-29 /pmc/articles/PMC8143733/ /pubmed/33928917 http://dx.doi.org/10.1097/CM9.0000000000001500 Text en Copyright © 2021 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Correspondence Wu, Juan Zhong, Lin Chen, Ting Qiu, Li Li, Yi-Fei A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 (PIEZO2) induced tracheobronchomalacia |
title | A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 (PIEZO2) induced tracheobronchomalacia |
title_full | A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 (PIEZO2) induced tracheobronchomalacia |
title_fullStr | A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 (PIEZO2) induced tracheobronchomalacia |
title_full_unstemmed | A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 (PIEZO2) induced tracheobronchomalacia |
title_short | A rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 (PIEZO2) induced tracheobronchomalacia |
title_sort | rare case with compound heterozygous mutations of piezo-type mechanosensitive ion channel component 2 (piezo2) induced tracheobronchomalacia |
topic | Correspondence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143733/ https://www.ncbi.nlm.nih.gov/pubmed/33928917 http://dx.doi.org/10.1097/CM9.0000000000001500 |
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