Investigation of the GJB6 Deletion Mutations Del (GJB6-D13s1830) and Del (GJB6-D13s1854) in Iranian Patients with Autosomal-Recessive Non-Syndromic Hearing Loss (ARNSHL)
Hearing loss (HL) is the most common inherited sensory disorder affecting about 1 in 1000 births. The first locus for nonsyndromic autosomal recessive HL is on chromosome 13q11-22. The two genes, GJB2 and GJB6, are closely located on chromosome and are known to be co-expressed in the embryonic cochl...
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Instituto de Tecnologia do Paraná (Tecpar)
2016-04-01
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| Colección: | Brazilian Archives of Biology and Technology |
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| Acceso en línea: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132016000100311&lng=en&tlng=en |
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