Prevalence of the 35delG mutation in the GJB2 gene in two samples of non-syndromic deaf subjects from Chile

Prevalence of the 35delG mutation in the GJB2 gene in two samples of non-syndromic deaf subjects from Chile

Hearing loss is the most common inherited sensorial deficiency in humans; about 1 in 1000 children suffer from severe or profound hearing loss at birth. Mutations in the GJB2 gene are the most common cause of prelingual, non-syndromic autosomal recessive deafness in many populations; the c.35delG mu...

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Autores principales: Cifuentes,Lucía, Arancibia,Margarita, Torrente,Mariela, Acuña,Mónica, Farfán,Corina, Ríos,Carolina
Lenguaje:English
Publicado: Sociedad de Biología de Chile 2013
Materias:
Genetic deafness
Hereditary hearing loss
35delG mutation frequency
GJB2 mutations
Chilean population
Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602013000300003
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