Order Article Reprints

Shan T, Mukhtar N, Ullah SH, Ullah A, Khan AA, Li Y, Wang M, Tehreem R, Aziz A, Afshan K, et al. Expanding the Mutation Spectrum of Non-Syndromic Retinitis Pigmentosa in Consanguineous Pakistani Families: Unraveling Novel Pathogenic Variants in RP1, PDE6B, and PRCD Genes for Precision Diagnosis. Genes. 2026; 17(5):529. https://doi.org/10.3390/genes17050529

Shan, Tayyaba, Nimra Mukhtar, Sayyed Hammad Ullah, Asad Ullah, Asfandyar Ahmad Khan, Yumei Li, Meng Wang, Raeesa Tehreem, Amtul Aziz, Kiran Afshan, and et al. 2026. "Expanding the Mutation Spectrum of Non-Syndromic Retinitis Pigmentosa in Consanguineous Pakistani Families: Unraveling Novel Pathogenic Variants in RP1, PDE6B, and PRCD Genes for Precision Diagnosis" Genes 17, no. 5: 529. https://doi.org/10.3390/genes17050529

Shan, T., Mukhtar, N., Ullah, S. H., Ullah, A., Khan, A. A., Li, Y., Wang, M., Tehreem, R., Aziz, A., Afshan, K., Chen, R., & Firasat, S. (2026). Expanding the Mutation Spectrum of Non-Syndromic Retinitis Pigmentosa in Consanguineous Pakistani Families: Unraveling Novel Pathogenic Variants in RP1, PDE6B, and PRCD Genes for Precision Diagnosis. Genes, 17(5), 529. https://doi.org/10.3390/genes17050529