EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss

BACKGROUND: More than 70 % of the cases of congenital deafness are of genetic origin, of which approximately 80 % are non-syndromic and show autosomal recessive transmission (DFNB forms). To date, 60 DFNB genes have been identified, most of which cause congenital, severe to profound deafness, wherea...

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Detalles Bibliográficos
Autores principales: Dahmani, Malika, Ammar-Khodja, Fatima, Bonnet, Crystel, Lefèvre, Gaelle M., Hardelin, Jean-Pierre, Ibrahim, Hassina, Mallek, Zahia, Petit, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539681/
https://www.ncbi.nlm.nih.gov/pubmed/26282398
http://dx.doi.org/10.1186/s13023-015-0316-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539681/
https://www.ncbi.nlm.nih.gov/pubmed/26282398
http://dx.doi.org/10.1186/s13023-015-0316-8

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