Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review

Autosomal dominant non-syndromic hearing loss (HL) typically occurs when only one dominant allele within the disease gene is sufficient to express the phenotype. Therefore, most patients diagnosed with autosomal dominant non-syndromic HL have a hearing-impaired parent, although de novo mutations sho...

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Detalles Bibliográficos
Autores principales: Aldè, Mirko, Cantarella, Giovanna, Zanetti, Diego, Pignataro, Lorenzo, La Mantia, Ignazio, Maiolino, Luigi, Ferlito, Salvatore, Di Mauro, Paola, Cocuzza, Salvatore, Lechien, Jérôme René, Iannella, Giannicola, Simon, Francois, Maniaci, Antonino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296186/
https://www.ncbi.nlm.nih.gov/pubmed/37371710
http://dx.doi.org/10.3390/biomedicines11061616

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296186/
https://www.ncbi.nlm.nih.gov/pubmed/37371710
http://dx.doi.org/10.3390/biomedicines11061616

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