Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3.
Stem cell research | 2024-06-01 | PMID 38479331
Mahato Sudipta, Maddileti Savitri, Naik Milind and 3 more
