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Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in PRPF31-associated retinopathy.
Roshandel D, Thompson JA, Charng J, Zhang D, Chelva E, Arunachalam S, Attia MS, Lamey TM, McLaren TL, De Roach JN, Mackey DA, Wilton SD, Fletcher S, McLenachan S, Chen FK. Roshandel D, et al. Among authors: zhang d. Ophthalmic Genet. 2021 Feb;42(1):1-14. doi: 10.1080/13816810.2020.1827442. Epub 2020 Sep 27. Ophthalmic Genet. 2021. PMID: 32985313
mRNA transfection of mouse and human neural stem cell cultures.
McLenachan S, Zhang D, Palomo AB, Edel MJ, Chen FK. McLenachan S, et al. Among authors: zhang d. PLoS One. 2013 Dec 26;8(12):e83596. doi: 10.1371/journal.pone.0083596. eCollection 2013. PLoS One. 2013. PMID: 24386231 Free PMC article.
Clinical and molecular characterization of non-syndromic retinal dystrophy due to c.175G>A mutation in ceroid lipofuscinosis neuronal 3 (CLN3).
Chen FK, Zhang X, Eintracht J, Zhang D, Arunachalam S, Thompson JA, Chelva E, Mallon D, Chen SC, McLaren T, Lamey T, De Roach J, McLenachan S. Chen FK, et al. Among authors: zhang d, zhang x. Doc Ophthalmol. 2019 Feb;138(1):55-70. doi: 10.1007/s10633-018-9665-7. Epub 2018 Nov 16. Doc Ophthalmol. 2019. PMID: 30446867
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