Screening for Genetic Mutations for the Early Diagnosis of Common Variable Immunodeficiency in Children With Refractory Immune Thrombocytopenia: A Retrospective Data Analysis From a Tertiary Children's Center

Aim: This study aimed to identify common variable immunodeficiency (CVID) by high-throughput next-generation sequencing (NGS) in children with refractory immune thrombocytopenia (RITP) to facilitate early diagnosis. Methods: CVID-related genetic mutations were explored in patients with RITP during 2...

Descripción completa

Detalles Bibliográficos
Autores principales: Ma, Jingyao, Fu, Lingling, Gu, Hao, Chen, Zhenping, Zhang, Jialu, Zhao, Shasha, Zhu, Xiaojing, Liu, Huiqing, Wu, Runhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793988/
https://www.ncbi.nlm.nih.gov/pubmed/33425813
http://dx.doi.org/10.3389/fped.2020.595135

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793988/
https://www.ncbi.nlm.nih.gov/pubmed/33425813
http://dx.doi.org/10.3389/fped.2020.595135

Ejemplares similares