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

Detalles Bibliográficos
Autores principales: Wu, Juan, Zhong, Lin, Chen, Ting, Qiu, Li, Li, Yi-Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
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
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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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