Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairment
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/article/10.1186/s12881-015-0145-6/fulltext.html
Reference36 articles.
1. Lehtonen MS, Uimonen S, Hassinen IE, Majamaa K. Frequency of mitochondrial DNA point mutations among patients with familial sensorineural hearing impairment. Eur J Hum Genet. 2000;8(4):315–8.
2. Majamaa K, Moilanen JS, Uimonen S, Remes AM, Salmela PI, Karppa M, et al. Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population. Am J Hum Genet. 1998;63(2):447–54.
3. Uusimaa J, Moilanen JS, Vainionpaa L, Tapanainen P, Lindholm P, Nuutinen M, et al. Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A > G mutation in children. Ann Neurol. 2007;62(3):278–87.
4. Bitner-Glindzicz M, Pembrey M, Duncan A, Heron J, Ring SM, Hall A, et al. Prevalence of mitochondrial 1555A– > G mutation in European children. N Engl J Med. 2009;360(6):640–2.
5. Manwaring N, Jones MM, Wang JJ, Rochtchina E, Howard C, Mitchell P, et al. Population prevalence of the MELAS A3243G mutation. Mitochondrion. 2007;7(3):230–3.
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