Yousaf, K.; Naz, S.; Mushtaq, A.; Wohler, E.; Sobreira, N.; Ho, B.-M.; Chen, L.-J.; Chu, W.-K.; Bashir, R.
Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma. Genes 2023, 14, 310.
https://doi.org/10.3390/genes14020310
AMA Style
Yousaf K, Naz S, Mushtaq A, Wohler E, Sobreira N, Ho B-M, Chen L-J, Chu W-K, Bashir R.
Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma. Genes. 2023; 14(2):310.
https://doi.org/10.3390/genes14020310
Chicago/Turabian Style
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, no. 2: 310.
https://doi.org/10.3390/genes14020310
APA Style
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
