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Ortore RP, Leone MP, Palumbo O, Petracca A, Trecca EMC, D’Ecclesia A, Vigliaroli CL, Micale L, Longo F, Melchionda S, et al. Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family. Audiology Research. 2021; 11(3):443-451. https://doi.org/10.3390/audiolres11030041

Ortore, Rocco Pio, Maria Pia Leone, Orazio Palumbo, Antonio Petracca, Eleonora M. C. Trecca, Aurelio D’Ecclesia, Ciro Lucio Vigliaroli, Lucia Micale, Francesco Longo, Salvatore Melchionda, and et al. 2021. "Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family" Audiology Research 11, no. 3: 443-451. https://doi.org/10.3390/audiolres11030041

Ortore, R. P., Leone, M. P., Palumbo, O., Petracca, A., Trecca, E. M. C., D’Ecclesia, A., Vigliaroli, C. L., Micale, L., Longo, F., Melchionda, S., & Castori, M. (2021). Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family. Audiology Research, 11(3), 443-451. https://doi.org/10.3390/audiolres11030041