Yu-qiu Zhou

LOVD–DASH: A comprehensive LOVD database coupled with diagnosis and an at‐risk assessment system for hemoglobinopathies

M. Qi, Shanhuo Yan, Yuehong Zhou, 2019, Human mutation.

DNA hypermethylation and X chromosome inactivation are major determinants of phenotypic variation in women heterozygous for G6PD mutations.

Xiang-min Xu, F. Xiong, Xiang-cai Wei, 2014, Blood cells, molecules & diseases.

Erythroid Krüppel-like factor mutations are relatively more common in a thalassemia endemic region and ameliorate the clinical and hematological severity of β-thalassemia

Tizhen Yan, Li Lin, N. Mohandas, 2014 .

KLF1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of β-thalassemia.

Tizhen Yan, Li Lin, N. Mohandas, 2014, Blood.

RED CELLS , IRON , AND ERYTHROPOIESIS KLF 1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of b-thalassemia

Tizhen Yan, Li Lin, N. Mohandas, 2014 .