A study of GJB2 and delGJB6-D13S1830 mutations in Brazilian non-syndromic deaf children from the Amazon region

Hearing impairment affects about 1 in 1000 newborns. Mutations in the connexin 26 (GJB2) gene rank among the most frequent causes of non-syndromic deafness in different populations, while delGJB6-D13S1830 mutation located in the DFNB30 locus is known to cause sensorineural hearing loss. Despite the...

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Detalles Bibliográficos
Autores principales: Castro, Luciana Santos Serrão de, Marinho, Anderson Nonato do Rosario, Rodrigues, Elzemar Martins Ribeiro, Marques, Giorgio Christie Tavares, Carvalho, Tarcísio André Amorim de, Silva, Luiz Carlos Santana da, Santos, Sidney Emanuel Batista dos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450865/
https://www.ncbi.nlm.nih.gov/pubmed/23503914
http://dx.doi.org/10.5935/1808-8694.20130016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450865/
https://www.ncbi.nlm.nih.gov/pubmed/23503914
http://dx.doi.org/10.5935/1808-8694.20130016

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