A Case of Adult Hereditary Spherocytosis Concomitant with Gilbert Syndrome Caused by Mutations in SPTB and UGT1A1

• Main Authors: Gou Y (Author), Wang P (Author), Yang W (Author), Feng Y (Author), Peng X (Author), Liu H (Author), Liu S (Author), Zhang X (Author)
• Format: Book
• Published: Dove Medical Press, 2024-09-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Yang Gou,1,2 Ping Wang,1,2 Wucheng Yang,1,2 Yimei Feng,1,2 Xiangui Peng,1,2 Hong Liu,1,2 Shuiqing Liu,1,2 Xi Zhang1,2 1Medical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, People's Republic of China; 2Chongqing Key Laboratory of Hematology and Microenvir...