A novel SPTB frameshift deletion causing hereditary spherocytosis identified by next-generation sequencing in a Chinese family

被引：2

作者：

Zhao, Ru-Qing ^{[1
]}

Jiang, Fan ^{[2
]}

Li, Jian ^{[2
]}

Zhou, Jian-Ying ^{[2
]}

Tang, Xue-Wei ^{[2
]}

Li, Fa-Tao ^{[2
]}

Chen, Li-Qiong ^{[1
]}

Li, Dong-Zhi ^{[2
]}

机构：

[1] Hexian Mem Med Hosp Panyu Dist, Panyu Maternal & Children Healthcare Hosp, Guangzhou, Peoples R China

[2] Guangzhou Women & Children Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Peoples R China

来源：

INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY | 2021年 / 43卷 / 06期

关键词：

hemolytic anemia; hereditary spherocytosis; GUIDELINES;

D O I：

10.1111/ijlh.13575

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：E294 / E297

页数：4

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