A novel SPTB frameshift deletion causing hereditary spherocytosis identified by next-generation sequencing in a Chinese family.
Ru-Qing ZhaoFan JiangJian LiJian-Ying ZhouXue-Wei TangFa-Tao LiLi-Qiong ChenDong-Zhi LiPublished in: International journal of laboratory hematology (2021)