Clinical manifestations and phenotypic analysis of new ANK1 gene mutations in 12 Chinese children with hereditary spherocytosis
Fei Xie, Lei Lei, Bin Cai, Lu Gan, Yu Gao, Xiaoying Liu, Lin Zhou, Jinjin Jiang
The paper identifies new ANK1 gene mutations in 12 Chinese children with hereditary spherocytosis and evaluates their clinical and genetic implications.
bioRxiv · May 15, 2019 · PreprintGenetics