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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
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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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 |
description | |
format | Online Article Text |
id | pubmed-8152414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
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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