Open AccessNovel SPTB frameshift mutation in a Chinese neonatal case of hereditary spherocytosis type 2: A case report
Author(s) -
Cunxin Xu,
Yangjie Wu,
Dujuan Wang,
Xuemin Zhang,
Ningling Wang
Publication year - 2022
Publication title -
experimental and therapeutic medicine
Language(s) - English
Resource type - Journals
eISSN - 1792-1015
pISSN - 1792-0981
DOI - 10.3892/etm.2022.11537
Subject(s) - frameshift mutation , hereditary spherocytosis , jaundice , medicine , ankyrin , mutation , pediatrics , phenotype , anemia , immunology , gastroenterology , genetics , gene , biology