Clinical and genetic characterisation of childhood-onset sensorineural hearing loss reveal associated phenotypes and enrichment of pathogenic founder mutations in the Finnish population.

MLA

Kraatari-Tiri, Minna, et al. “Clinical and Genetic Characterisation of Childhood-Onset Sensorineural Hearing Loss Reveal Associated Phenotypes and Enrichment of Pathogenic Founder Mutations in the Finnish Population.” International Journal of Audiology, Oct. 2024, pp. 1–6. EBSCOhost, https://doi.org/10.1080/14992027.2024.2402840.

APA

Kraatari-Tiri, M., Pykälainen, T., Pohjola, P., Häkli, S., & Rahikkala, E. (2024). Clinical and genetic characterisation of childhood-onset sensorineural hearing loss reveal associated phenotypes and enrichment of pathogenic founder mutations in the Finnish population. International Journal of Audiology, 1–6. https://doi.org/10.1080/14992027.2024.2402840

Chicago

Kraatari-Tiri, Minna, Tyrni Pykälainen, Pia Pohjola, Sanna Häkli, and Elisa Rahikkala. 2024. “Clinical and Genetic Characterisation of Childhood-Onset Sensorineural Hearing Loss Reveal Associated Phenotypes and Enrichment of Pathogenic Founder Mutations in the Finnish Population.” International Journal of Audiology, October, 1–6. doi:10.1080/14992027.2024.2402840.