Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis

PURPOSE: Objective to summarize the clinical features and laboratory findings of 28 Chinese children with hereditary spherocytosis (HS), and analyze these mutations. METHOD: Collected and analyzed the clinical data of all children and their parents, and completed the relevant laboratory examinations...

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Detalles Bibliográficos
Autores principales: Xie, Fei, Lei, Lei, Cai, Bin, Gan, Lu, Gao, Yu, Liu, Xiaoying, Zhou, Lin, Jiang, Jinjin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123760/
https://www.ncbi.nlm.nih.gov/pubmed/33620149
http://dx.doi.org/10.1002/mgg3.1577

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123760/
https://www.ncbi.nlm.nih.gov/pubmed/33620149
http://dx.doi.org/10.1002/mgg3.1577

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