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Determinants of Disease Penetrance in PRPF31-Associated Retinopathy.
McLenachan S, Zhang D, Grainok J, Zhang X, Huang Z, Chen SC, Zaw K, Lima A, Jennings L, Roshandel D, Moon SY, Heath Jeffery RC, Attia MS, Thompson JA, Lamey TM, McLaren TL, De Roach J, Fletcher S, Chen FK. McLenachan S, et al. Among authors: zhang d, zhang x. Genes (Basel). 2021 Sep 28;12(10):1542. doi: 10.3390/genes12101542. Genes (Basel). 2021. PMID: 34680937 Free PMC article.
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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