Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene

Hearing loss (HL) is the most frequent sensory disorder, affecting about 1–3 per 1000 live births, with more than half of the cases attributable to genetic causes. Despite the fact that many HL causative genes have already been identified, current genetic tests fail to provide a diagnosis for about...

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Detalles Bibliográficos
Autores principales: Tesolin, Paola, Morgan, Anna, Notarangelo, Michela, Ortore, Rocco Pio, Concas, Maria Pina, Notarangelo, Angelantonio, Girotto, Giorgia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304864/
https://www.ncbi.nlm.nih.gov/pubmed/34356059
http://dx.doi.org/10.3390/genes12071043

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304864/
https://www.ncbi.nlm.nih.gov/pubmed/34356059
http://dx.doi.org/10.3390/genes12071043

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