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A novel gene mutation in a family with X-linked retinoschisis.
Lai YH, Huang SP, Chen SP, Hu PS, Lin SF, Sheu MM, Wang HZ, Tsai RK. Lai YH, et al. Among authors: huang sp. J Formos Med Assoc. 2015 Sep;114(9):872-80. doi: 10.1016/j.jfma.2014.01.001. Epub 2014 Feb 13. J Formos Med Assoc. 2015. PMID: 24529551 Free article.
Gene therapy in hereditary retinal dystrophy.
Chien JY, Huang SP. Chien JY, et al. Among authors: huang sp. Tzu Chi Med J. 2022 Aug 23;34(4):367-372. doi: 10.4103/tcmj.tcmj_78_22. eCollection 2022 Oct-Dec. Tzu Chi Med J. 2022. PMID: 36578644 Free PMC article. Review.
Highly efficient capture approach for the identification of diverse inherited retinal disorders.
Kao HJ, Lin TY, Hsieh FJ, Chien JY, Yeh EC, Lin WJ, Chen YH, Ding KH, Yang Y, Chi SC, Tsai PH, Hsu CC, Hwang DK, Tsai HY, Peng ML, Lee SH, Chau SF, Chen CY, Cheang WM, Chen SJ, Kwok PY, Chiou SH, Lu MJ, Huang SP. Kao HJ, et al. Among authors: huang sp. NPJ Genom Med. 2024 Jan 9;9(1):4. doi: 10.1038/s41525-023-00388-3. NPJ Genom Med. 2024. PMID: 38195571 Free PMC article.
656 results