Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3
Leber congenital amaurosis (LCA) is a congenital, early onset, autosomal recessive inherited retinal disease (IRD). This report describes an LCA12 patient-specific iPSC line (LVPEIi006-A), generated by the reprogramming of dermal fibroblasts using integration-free episomal plasmids.This disease-spec...
Main Authors: | Sudipta Mahato, Savitri Maddileti, Milind Naik, Chitra Kannabiran, Subhadra Jalali, Indumathi Mariappan |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2024-06-01
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Series: | Stem Cell Research |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1873506124000783 |
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