Clinical report and genetic analysis of a Chinese family with retinitis pigmentosa 79 caused by a novel loss-of-function HK1 variant.

MLA

Luo, Xin, et al. “Clinical Report and Genetic Analysis of a Chinese Family with Retinitis Pigmentosa 79 Caused by a Novel Loss-of-Function HK1 Variant.” Genes & Genomics, vol. 46, no. 12, Dec. 2024, pp. 1437–44. EBSCOhost, https://doi.org/10.1007/s13258-024-01574-y.

APA

Luo, X., Wang, L., & Xue, D. (2024). Clinical report and genetic analysis of a Chinese family with retinitis pigmentosa 79 caused by a novel loss-of-function HK1 variant. Genes & Genomics, 46(12), 1437–1444. https://doi.org/10.1007/s13258-024-01574-y

Chicago

Luo, Xin, Lu Wang, and Daxi Xue. 2024. “Clinical Report and Genetic Analysis of a Chinese Family with Retinitis Pigmentosa 79 Caused by a Novel Loss-of-Function HK1 Variant.” Genes & Genomics 46 (12): 1437–44. doi:10.1007/s13258-024-01574-y.