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Mitochondrial DNA Mutation Screening in an Ethnically Diverse Nonsyndromic Deafness Cohort
Deafness is a heterogeneous trait with many known genetic and environmental causes. Hereditary hearing loss is an extremely common disorder in the general population. Mutations in mitochondrial DNA (mtDNA) are known to be associated with nonsyndromic deafness (NSD) and syndromic deafness. The object...
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| Huvudupphovsmän: | , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Mary Ann Liebert, Inc.
2012
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3438807/ https://ncbi.nlm.nih.gov/pubmed/22853457 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2011.0365 |
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