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Dyskeratosis Congenita with DKC1 Mutation: A Case Report

Detalles Bibliográficos
Autores principales: Zhao, Xing-Yun, Zhong, Wei-Long, Zhang, Jie, Ma, Gang, Hu, Hao, Yu, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7640797/
https://www.ncbi.nlm.nih.gov/pubmed/33165394
http://dx.doi.org/10.4103/ijd.IJD_716_18
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author Zhao, Xing-Yun
Zhong, Wei-Long
Zhang, Jie
Ma, Gang
Hu, Hao
Yu, Bo
author_facet Zhao, Xing-Yun
Zhong, Wei-Long
Zhang, Jie
Ma, Gang
Hu, Hao
Yu, Bo
author_sort Zhao, Xing-Yun
collection PubMed
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spelling pubmed-76407972020-11-05 Dyskeratosis Congenita with DKC1 Mutation: A Case Report Zhao, Xing-Yun Zhong, Wei-Long Zhang, Jie Ma, Gang Hu, Hao Yu, Bo Indian J Dermatol Correspondences Wolters Kluwer - Medknow 2020 /pmc/articles/PMC7640797/ /pubmed/33165394 http://dx.doi.org/10.4103/ijd.IJD_716_18 Text en Copyright: © 2020 Indian Journal of Dermatology http://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 Correspondences
Zhao, Xing-Yun
Zhong, Wei-Long
Zhang, Jie
Ma, Gang
Hu, Hao
Yu, Bo
Dyskeratosis Congenita with DKC1 Mutation: A Case Report
title Dyskeratosis Congenita with DKC1 Mutation: A Case Report
title_full Dyskeratosis Congenita with DKC1 Mutation: A Case Report
title_fullStr Dyskeratosis Congenita with DKC1 Mutation: A Case Report
title_full_unstemmed Dyskeratosis Congenita with DKC1 Mutation: A Case Report
title_short Dyskeratosis Congenita with DKC1 Mutation: A Case Report
title_sort dyskeratosis congenita with dkc1 mutation: a case report
topic Correspondences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7640797/
https://www.ncbi.nlm.nih.gov/pubmed/33165394
http://dx.doi.org/10.4103/ijd.IJD_716_18
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