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Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome

Detalles Bibliográficos
Autores principales: Huang, Chuan, Liu, Na-Chuan, Wang, Xiao-Bo, Gu, Ben-Hong, Zhang, Jian-Xiong, Li-Zhang, Li, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152414/
https://www.ncbi.nlm.nih.gov/pubmed/33106461
http://dx.doi.org/10.4103/aja.aja_43_20
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author Huang, Chuan
Liu, Na-Chuan
Wang, Xiao-Bo
Gu, Ben-Hong
Zhang, Jian-Xiong
Li-Zhang,
Li, Zheng
author_facet Huang, Chuan
Liu, Na-Chuan
Wang, Xiao-Bo
Gu, Ben-Hong
Zhang, Jian-Xiong
Li-Zhang,
Li, Zheng
author_sort Huang, Chuan
collection PubMed
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spelling pubmed-81524142021-06-02 Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome Huang, Chuan Liu, Na-Chuan Wang, Xiao-Bo Gu, Ben-Hong Zhang, Jian-Xiong Li-Zhang, Li, Zheng Asian J Androl Letter to the Editor Wolters Kluwer - Medknow 2020-10-20 /pmc/articles/PMC8152414/ /pubmed/33106461 http://dx.doi.org/10.4103/aja.aja_43_20 Text en Copyright: ©The Author(s)(2020) https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Letter to the Editor
Huang, Chuan
Liu, Na-Chuan
Wang, Xiao-Bo
Gu, Ben-Hong
Zhang, Jian-Xiong
Li-Zhang,
Li, Zheng
Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome
title Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome
title_full Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome
title_fullStr Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome
title_full_unstemmed Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome
title_short Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome
title_sort novel deletion mutations of the pih1d3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with kartagener's syndrome
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152414/
https://www.ncbi.nlm.nih.gov/pubmed/33106461
http://dx.doi.org/10.4103/aja.aja_43_20
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