Article Versions Notes

Hassan AY, Yousaf S, Levin MR, Saeedi OJ, Riazuddin S, Alexander JL, Ahmed ZM. Novel Homozygous Missense Variant in GJA3 Connexin Domain Causing Congenital Nuclear and Cortical Cataracts. International Journal of Molecular Sciences. 2022; 23(1):240. https://doi.org/10.3390/ijms23010240

Hassan, Abdullah Y., Sairah Yousaf, Moran R. Levin, Osamah J. Saeedi, Saima Riazuddin, Janet L. Alexander, and Zubair M. Ahmed. 2022. "Novel Homozygous Missense Variant in GJA3 Connexin Domain Causing Congenital Nuclear and Cortical Cataracts" International Journal of Molecular Sciences 23, no. 1: 240. https://doi.org/10.3390/ijms23010240

Hassan, A. Y., Yousaf, S., Levin, M. R., Saeedi, O. J., Riazuddin, S., Alexander, J. L., & Ahmed, Z. M. (2022). Novel Homozygous Missense Variant in GJA3 Connexin Domain Causing Congenital Nuclear and Cortical Cataracts. International Journal of Molecular Sciences, 23(1), 240. https://doi.org/10.3390/ijms23010240