Molecular genetics of non-syndromic deafness

One in every 1,000 newborn suffers from congenital hearing impairment. More than 60% of the congenital cases are caused by genetic factors. In most cases, hearing loss is a multifactorial disorder caused by both genetic and environmental factors. Molecular genetics of deafness has experienced remark...

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Detalles Bibliográficos
Autores principales: Piatto, Vânia B., Nascimento, Ellen C.T., Alexandrino, Fabiana, Oliveira, Camila A., Lopes, Ana Cláudia P., Sartorato, Edi Lúcia, Maniglia, José Victor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450533/
https://www.ncbi.nlm.nih.gov/pubmed/16446920
http://dx.doi.org/10.1016/S1808-8694(15)31313-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450533/
https://www.ncbi.nlm.nih.gov/pubmed/16446920
http://dx.doi.org/10.1016/S1808-8694(15)31313-6

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