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References
These sources were used to develop the Genetics Home Reference
gene summary
on the
MT-RNR1
gene.
Entrez
Gene
Fischel-Ghodsian N, Kopke RD, Ge X. Mitochondrial dysfunction in hearing loss. Mitochondrion. 2004 Sep;4(5-6):675-94. Epub 2004 Nov 6.
PubMed citation
Fischel-Ghodsian N. Genetic factors in aminoglycoside toxicity. Pharmacogenomics. 2005 Jan;6(1):27-36. Review.
PubMed citation
Fischel-Ghodsian N. Mitochondrial deafness. Ear Hear. 2003 Aug;24(4):303-13. Review.
PubMed citation
Gene Review: Nonsyndromic Hearing Loss and Deafness,
Mitochondrial
Giordano C, Pallotti F, Walker WF, Checcarelli N, Musumeci O, Santorelli F, d'Amati G, Schon EA, DiMauro S, Hirano M, Davidson MM. Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation. Biochem Biophys Res Commun. 2002 Apr 26;293(1):521-9.
PubMed citation
Guan MX. Molecular pathogenetic mechanism of maternally inherited deafness. Ann N Y Acad Sci. 2004 Apr;1011:259-71.
PubMed citation
Van Camp G, Smith RJ. Maternally inherited hearing impairment. Clin Genet. 2000 Jun;57(6):409-14. Review.
PubMed citation
Zhao H, Young WY, Yan Q, Li R, Cao J, Wang Q, Li X, Peters JL, Han D, Guan MX. Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss. Nucleic Acids Res. 2005 Feb 18;33(3):1132-9. Print 2005.
PubMed citation
Reviewed: November 2006
Published: May 20, 2013
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