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Genetics of non syndromic hearing loss
Non Syndromic Hearing Loss is an important cause for hearing loss. One in 1000 newborns have some hearing impairment. Over 400 genetic syndromes have been described. Non Syndromic Hearing Loss (NSHL) can be inherited in an Autosomal Dominant, Autosomal Recessive or a Sex Linked fashion. There are se...
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| I publikationen: | Med J Armed Forces India |
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| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Elsevier
2015
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4646903/ https://ncbi.nlm.nih.gov/pubmed/26663965 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mjafi.2015.07.003 |
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