Zha, C., Farah, C. A., Holt, R. J., Ceroni, F., Al-Abdi, L., Thuriot, F., . . . Sossin, W. S. (2020). Biallelic variants in the small optic lobe calpain CAPN15 are associated with congenital eye anomalies, deafness and other neurodevelopmental deficits. Hum Mol Genet.

Zha, Congyao, et al. "Biallelic Variants in the Small Optic Lobe Calpain CAPN15 Are Associated With Congenital Eye Anomalies, Deafness and Other Neurodevelopmental Deficits." Hum Mol Genet 2020.

Zha, Congyao, et al. "Biallelic Variants in the Small Optic Lobe Calpain CAPN15 Are Associated With Congenital Eye Anomalies, Deafness and Other Neurodevelopmental Deficits." Hum Mol Genet 2020.