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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Bibliographic Details
Main Authors: Vivero, Richard J., Ouyang, Xiaomei, Yan, Denise, Du, Lilin, Liu, Wendy, Angeli, Simon I., Liu, Xue Zhong
Format: Artigo
Language:Inglês
Published: Mary Ann Liebert, Inc. 2012
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Short Reports
Online Access: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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