Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma.

MLA

Yousaf, Khazeema, et al. “Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma.” Genes, vol. 14, no. 2, Feb. 2023, p. 310. EBSCOhost, https://doi.org/10.3390/genes14020310.

APA

Yousaf, K., Naz, S., Mushtaq, A., Wohler, E., Sobreira, N., Ho, B.-M., Chen, L.-J., Chu, W.-K., & Bashir, R. (2023). Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma. Genes, 14(2), 310. https://doi.org/10.3390/genes14020310

Chicago

Yousaf, Khazeema, Sadaf Naz, Asma Mushtaq, Elizabeth Wohler, Nara Sobreira, Bo-Man Ho, Li-Jia Chen, Wai-Kit Chu, and Rasheeda Bashir. 2023. “Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma.” Genes 14 (2): 310. doi:10.3390/genes14020310.