1. Clinical and molecular characteristics of Wiskott‐Aldrich Syndrome in five unrelated Chinese families. (16th November 2021) Authors: Jiang, Jiali; Zhou, Junli; Wei, Manlv; Singh, Sanjeev; Nikuze, Lauriane; Huang, Lifang; Li, Yuping; Jiang, Jinxia; Wei, Hongying Journal: Scandinavian journal of immunology Issue: Volume 95:Number 1(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Identification of one novel pathogenic ITGB3 mutation and two known mutations in two Chinese pedigrees with hereditary Glanzmann thrombasthenia. (2nd April 2020) Authors: Lu, Zhengjing; Nikuze, Lauriane; Zhong, Zhoulin; Li, Fang; Zhang, Fuyong; Liang, Kairong; Wei, Manlv; Wei, Hongying Journal: Platelets Issue: Volume 31:Number 3(2020) Page Start: 355 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Identification of two novel mutations in three children with congenital factor VII deficiency. Issue 5 (July 2021) Authors: Liang, Kairong; Nikuze, Lauriane; Zhang, Fuyong; Lu, Zhengjing; Wei, Manlv; Wei, Hongying Journal: Blood coagulation and fibrinolysis Issue: Volume 32:Issue 5(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗