Gene Therapy for Sickle Cell Disease, β-Thalassemia Enters Regulatory Reviews
Author:
Publisher
American Medical Association (AMA)
Subject
General Medicine
Link
https://jamanetwork.com/journals/jama/articlepdf/2798189/jama_larkin_2022_bi_220029_1667495615.52815.pdf
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. CRISPR technology in human diseases;MedComm;2024-07-29
2. HLA haplotype frequencies and diversity in patients with hemoglobinopathies;eJHaem;2023-08-04
3. Logistic‐Nomogram model based on red blood cell parameters to differentiate thalassemia trait and iron deficiency anemia in southern region of Fujian Province, China;Journal of Clinical Laboratory Analysis;2023-06
4. Cell-based Genetic Therapy for the Induction of Foetal Haemoglobin in Sickle Cell Disease and Transfusion-dependent β-thalassaemia;Oncology & Haematology;2023
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