Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort

OBJECTIVE: Hereditary hearing loss (HL) is the most common sensorineural disorder in humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 gene have been reported as a cause of hereditary HL due to its role in the physiology of the inner ear. In this research we wanted...

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Detalles Bibliográficos
Autores principales: Carvalho, Simone da Costa e Silva, Grangeiro, Carlos Henrique Paiva, Picanço-Albuquerque, Clarissa Gondim, dos Anjos, Thaís Oliveira, De Molfetta, Greice Andreotti, Silva, Wilson Araujo, Ferraz, Victor Evangelista de Faria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071330/
https://www.ncbi.nlm.nih.gov/pubmed/30068397
http://dx.doi.org/10.1186/s13104-018-3647-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071330/
https://www.ncbi.nlm.nih.gov/pubmed/30068397
http://dx.doi.org/10.1186/s13104-018-3647-4

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