Gene Repair of iPSC Line with GARS (G294R) Mutation of CMT2D Disease by CRISPR/Cas9
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Biochemistry
Link
https://link.springer.com/content/pdf/10.1007/s11596-023-2707-8.pdf
Reference17 articles.
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2. Peretti A, Perie M, Vincent D, et al. LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2. Eur J Hum Genet, 2019,27(9):1406–1418
3. Sleigh JN, Dawes JM, West SJ, et al. Trk receptor signaling and sensory neuron fate are perturbed in human neuropathy caused by Gars mutations. Proc Natl Acad Sci USA, 2017,114(16):E3324–E3333
4. Mo Z, Zhao X, Liu H, et al. Aberrant GlyRS-HDAC6 interaction linked to axonal transport deficits in Charcot-Marie-Tooth neuropathy. Nat Commun, 2018,9(1):1007
5. Yoshida Y, Yamanaka S. Induced Pluripotent Stem Cells 10 Years Later: For Cardiac Applications. Circ Res, 2017,120(12):1958–1968
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