Severe congenital hemolytic anemia caused by a novel compound heterozygous PKLR gene mutation in a Chinese boy

Detalles Bibliográficos
Autores principales: Liu, Peng-Peng, Ding, Hu-Qing, Huang, Shen-Zhen, Yang, Sheng-Yong, Liu, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Correspondence
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629312/
https://www.ncbi.nlm.nih.gov/pubmed/30628965
http://dx.doi.org/10.1097/CM9.0000000000000027
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author Liu, Peng-Peng
Ding, Hu-Qing
Huang, Shen-Zhen
Yang, Sheng-Yong
Liu, Ting
author_facet Liu, Peng-Peng
Ding, Hu-Qing
Huang, Shen-Zhen
Yang, Sheng-Yong
Liu, Ting
author_sort Liu, Peng-Peng
collection PubMed
description
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spelling pubmed-66293122019-07-22 Severe congenital hemolytic anemia caused by a novel compound heterozygous PKLR gene mutation in a Chinese boy Liu, Peng-Peng Ding, Hu-Qing Huang, Shen-Zhen Yang, Sheng-Yong Liu, Ting Chin Med J (Engl) Correspondence Wolters Kluwer Health 2019-01-05 2019-01-05 /pmc/articles/PMC6629312/ /pubmed/30628965 http://dx.doi.org/10.1097/CM9.0000000000000027 Text en Copyright © 2018 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. http://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
spellingShingle Correspondence
Liu, Peng-Peng
Ding, Hu-Qing
Huang, Shen-Zhen
Yang, Sheng-Yong
Liu, Ting
Severe congenital hemolytic anemia caused by a novel compound heterozygous PKLR gene mutation in a Chinese boy
title Severe congenital hemolytic anemia caused by a novel compound heterozygous PKLR gene mutation in a Chinese boy
title_full Severe congenital hemolytic anemia caused by a novel compound heterozygous PKLR gene mutation in a Chinese boy
title_fullStr Severe congenital hemolytic anemia caused by a novel compound heterozygous PKLR gene mutation in a Chinese boy
title_full_unstemmed Severe congenital hemolytic anemia caused by a novel compound heterozygous PKLR gene mutation in a Chinese boy
title_short Severe congenital hemolytic anemia caused by a novel compound heterozygous PKLR gene mutation in a Chinese boy
title_sort severe congenital hemolytic anemia caused by a novel compound heterozygous pklr gene mutation in a chinese boy
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629312/
https://www.ncbi.nlm.nih.gov/pubmed/30628965
http://dx.doi.org/10.1097/CM9.0000000000000027
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