Lights and Shadows in the Genetics of Syndromic and Non-Syndromic Hearing Loss in the Italian Population

Hearing loss (HL), both syndromic (SHL) and non-syndromic (NSHL), is the most common sensory disorder, affecting ~460 million people worldwide. More than 50% of the congenital/childhood cases are attributable to genetic causes, highlighting the importance of genetic testing in this class of disorder...

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Detalles Bibliográficos
Autores principales: Morgan, Anna, Lenarduzzi, Stefania, Spedicati, Beatrice, Cattaruzzi, Elisabetta, Murru, Flora Maria, Pelliccione, Giulia, Mazzà, Daniela, Zollino, Marcella, Graziano, Claudio, Ambrosetti, Umberto, Seri, Marco, Faletra, Flavio, Girotto, Giorgia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690429/
https://www.ncbi.nlm.nih.gov/pubmed/33105617
http://dx.doi.org/10.3390/genes11111237

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