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Genetics of Nonsyndromic Congenital Hearing Loss

Congenital hearing impairment affects nearly 1 in every 1000 live births and is the most frequent birth defect in developed societies. Hereditary types of hearing loss account for more than 50% of all congenital sensorineural hearing loss cases and are caused by genetic mutations. HL can be either n...

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Sparad:
Bibliografiska uppgifter
I publikationen:Scientifica (Cairo)
Huvudupphovsmän: Egilmez, Oguz Kadir, Kalcioglu, M. Tayyar
Materialtyp: Artigo
Språk:Inglês
Publicerad: Hindawi Publishing Corporation 2016
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4775805/
https://ncbi.nlm.nih.gov/pubmed/26989561
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/7576064
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