Order Article Reprints

Borgese N, Guillén-Samander A, Colombo SF, Mancassola G, Di Berardino F, Zanetti D, Carrera P. Combined Presence in Heterozygosis of Two Variant Usher Syndrome Genes in Two Siblings Affected by Isolated Profound Age-Related Hearing Loss. Biomedicines. 2023; 11(10):2657. https://doi.org/10.3390/biomedicines11102657

Borgese, Nica, Andrés Guillén-Samander, Sara Francesca Colombo, Giulia Mancassola, Federica Di Berardino, Diego Zanetti, and Paola Carrera. 2023. "Combined Presence in Heterozygosis of Two Variant Usher Syndrome Genes in Two Siblings Affected by Isolated Profound Age-Related Hearing Loss" Biomedicines 11, no. 10: 2657. https://doi.org/10.3390/biomedicines11102657

Borgese, N., Guillén-Samander, A., Colombo, S. F., Mancassola, G., Di Berardino, F., Zanetti, D., & Carrera, P. (2023). Combined Presence in Heterozygosis of Two Variant Usher Syndrome Genes in Two Siblings Affected by Isolated Profound Age-Related Hearing Loss. Biomedicines, 11(10), 2657. https://doi.org/10.3390/biomedicines11102657