Linkage study of DFNB3 responsible for hearing loss in human

BACKGROUND: Hearing disorders represent a significant health problem worldwide. Recessive inherited cases of the deafness are more prevalent in Pakistan due to consanguineous marriages. Deafness caused by DFNB3 is due to mutation in the gene MYO XVA and its prevalence among Pakistani population is a...

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Detalles Bibliográficos
Autores principales: Ali, Akhtar, Babar, Masroor E., Kalsoom, Saeeda, Ahmad, Jamil, Abbas, Kamran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841558/
https://www.ncbi.nlm.nih.gov/pubmed/24339546
http://dx.doi.org/10.4103/0971-6866.120827

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841558/
https://www.ncbi.nlm.nih.gov/pubmed/24339546
http://dx.doi.org/10.4103/0971-6866.120827

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