The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population

Otosclerosis, the single most common cause of hearing impairment in white adults, is characterised by bone dystrophy localized to the otic capsule and isolated endochondral bone sclerosis with alternating phases of bone resorption and formation. Conductive hearing loss develops when otosclerotic foc...

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Detalles Bibliográficos
Autores principales: IOSSA, S., CORVINO, V., GIANNINI, P., SALVATO, R., CAVALIERE, M., PANETTI, M., PANETTI, G., PIANTEDOSI, B., MARCIANO, E., FRANZÈ, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pacini Editore SpA 2013
Materias:
Otology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825038/
https://www.ncbi.nlm.nih.gov/pubmed/24227897

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825038/
https://www.ncbi.nlm.nih.gov/pubmed/24227897

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