Audiologic and Genetic Features of the A3243G mtDNA Mutation

Background: Mitochondrial mutations have been shown to be responsible for syndromic and nonsyndromic hearing impairment. Aim: To assess the genotypic–phenotypic correlation of mitochondrial DNA mutations in three generations of a single family. Methods: A single family with maternally inherited diab...

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Hlavní autoři: Vivero, Richard J., Ouyang, Xiaomei, Kim, Yeunjung Grant, Liu, Wendy, Du, Lilin, Yan, Denise, Liu, Xue Zhong
Médium: Artigo
Jazyk:Inglês
Vydáno: Mary Ann Liebert, Inc. 2013
Témata:
Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3634140/
https://ncbi.nlm.nih.gov/pubmed/23477312
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2012.0403
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