Biblio

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Moon SYoon, Zhang D, Chen S-C, Lamey TM, Thompson JA, McLaren TL, De Roach JN, Chen FK, McLenachan S. Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1. Stem Cell Res. 2021;54:102403.

Zhang D, McLenachan S, Chen S-C, Zaw K, Alziyadat Y, Zhang X, Lamey TM, Thompson JA, McLaren TL, Mellough C, et al. Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200. Stem Cell Res. 2021;51:102154.

Huang D, Zhang D, Chen S-C, Aung-Htut MThandar, Lamey TM, Thompson JA, McLaren TL, De Roach JN, Fletcher S, Wilton SD, et al. Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 gene. Stem Cell Res. 2021;54:102448.

Huang D, Zhang D, Chen S-C, Aung-Htut MThandar, Lamey TM, Thompson JA, McLaren TL, De Roach JN, Fletcher S, Wilton SD, et al. Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461-10T>C;5603A>T];[6077T>C] mutations in the ABCA4 gene. Stem Cell Res. 2021;54:102439.

Zhang X, Zhang D, Thompson JA, Chen S-C, Huang Z, Jennings L, McLaren TL, Lamey TM, De Roach JN, Chen FK, et al. Gene correction of the CLN3 c.175G>A variant in patient-derived induced pluripotent stem cells prevents pathological changes in retinal organoids. Mol Genet Genomic Med. 2021:e1601.