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Macular dystrophies associated with Stargardt-like phenotypes.
Amaral RAS, Zin OA, Salles MV, Motta FL, Sallum JMF. Amaral RAS, et al. Among authors: sallum jmf. Arq Bras Oftalmol. 2023 Mar 24:S0004-27492023005002303. doi: 10.5935/0004-2749.2021-0415. Online ahead of print. Arq Bras Oftalmol. 2023. PMID: 36995812 Free article.
[Gene therapy for inherited retinal dystrophies].
Côco M, Han SW, Sallum JM. Côco M, et al. Arq Bras Oftalmol. 2009 Jul-Aug;72(4):560-6. doi: 10.1590/s0004-27492009000400026. Arq Bras Oftalmol. 2009. PMID: 19820803 Free article. Review. Portuguese.
Leveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants among exon-captured variants of uncertain significance.
Soens ZT, Branch J, Wu S, Yuan Z, Li Y, Li H, Wang K, Xu M, Rajan L, Motta FL, Simões RT, Lopez-Solache I, Ajlan R, Birch DG, Zhao P, Porto FB, Sallum J, Koenekoop RK, Sui R, Chen R. Soens ZT, et al. Hum Mutat. 2017 Nov;38(11):1521-1533. doi: 10.1002/humu.23294. Epub 2017 Aug 18. Hum Mutat. 2017. PMID: 28714225 Free PMC article.
Gene panel sequencing in Brazilian patients with retinitis pigmentosa.
Costa KA, Salles MV, Whitebirch C, Chiang J, Sallum JMF. Costa KA, et al. Among authors: sallum jmf. Int J Retina Vitreous. 2017 Sep 11;3:33. doi: 10.1186/s40942-017-0087-6. eCollection 2017. Int J Retina Vitreous. 2017. PMID: 28912962 Free PMC article.
65 results