Molecular Phenotype of a Human Lymphoblastoid Cell-line Homoplasmic for the np 7445 Deafness-associated Mitochondrial Mutation
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/6/3/443/1706397/6-3-443.pdf
Reference30 articles.
1. Epigenetic inheritance in mammals
2. A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness
3. Mitochondrial mutation associated with nonsyndromic deafness
4. Complete mtDNA sequence of a patient in a maternal pedigree with sensorineruar deatiness
5. Sequence and organization of the human mitochondrial genome
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2. Prevalence of mitochondrial DNA mutations in sporadic patients with nonsyndromic sensorineural hearing loss;Brazilian Journal of Otorhinolaryngology;2016-07
3. The Role of Mitochondrial DNA Mutations in Hearing Loss;Biochemical Genetics;2013-04-21
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