Generation of two induced pluripotent stem cell lines from Duchenne muscular dystrophy patients
Author:
Funder
National Institutes of Health
U.S. Food and Drug Administration
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference5 articles.
1. Duchenne muscular dystrophy;Duan;Nat. Rev. Dis. Primers,2021
2. Therapy for Duchenne muscular dystrophy: renewed optimism from genetic approaches;Fairclough;Nat. Rev. Genet.,2013
3. Evaluating the potential of novel genetic approaches for the treatment of Duchenne muscular dystrophy;Himic;Eur. J. Hum. Genet.,2021
4. Therapeutic developments for Duchenne muscular dystrophy;Verhaart;Nat. Rev. Neurol.,2019
5. Generation of two induced pluripotent stem cell lines from spinal muscular atrophy type 1 patients carrying no functional copies of SMN1 gene;Zeng;Stem Cell Res.,2023
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