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Genotype-Specific Lesion Growth Rates in Stargardt Disease.
Heath Jeffery RC, Thompson JA, Lo J, Lamey TM, McLaren TL, McAllister IL, Constable IJ, De Roach JN, Chen FK. Heath Jeffery RC, et al. Among authors: constable ij. Genes (Basel). 2021 Dec 14;12(12):1981. doi: 10.3390/genes12121981. Genes (Basel). 2021. PMID: 34946930 Free PMC article.
Leveraging natural history biorepositories as a global, decentralized, pathogen surveillance network.
Colella JP, Bates J, Burneo SF, Camacho MA, Carrion Bonilla C, Constable I, D'Elía G, Dunnum JL, Greiman S, Hoberg EP, Lessa E, Liphardt SW, Londoño-Gaviria M, Losos E, Lutz HL, Ordóñez Garza N, Peterson AT, Martin ML, Ribas CC, Struminger B, Torres-Pérez F, Thompson CW, Weksler M, Cook JA. Colella JP, et al. Among authors: constable i. PLoS Pathog. 2021 Jun 3;17(6):e1009583. doi: 10.1371/journal.ppat.1009583. eCollection 2021 Jun. PLoS Pathog. 2021. PMID: 34081744 Free PMC article.
A novel phenotype in a family with autosomal dominant retinal dystrophy due to c.1430A > G in retinoid isomerohydrolase (RPE65) and c.37C > T in bestrophin 1 (BEST1).
Pappalardo J, Heath Jeffery RC, Thompson JA, Chelva E, Pham Q, Constable IJ, McLaren TL, Lamey TM, De Roach JN, Chen FK. Pappalardo J, et al. Among authors: constable ij. Doc Ophthalmol. 2021 Aug;143(1):61-73. doi: 10.1007/s10633-021-09819-x. Epub 2021 Jan 29. Doc Ophthalmol. 2021. PMID: 33512609
319 results