Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.

Author:

Pandya A,Xia X,Radnaabazar J,Batsuuri J,Dangaansuren B,Fischel-Ghodsian N,Nance W E

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. Unique inheritance of streptomycin-induced deafness;Higashi, K.;Clin Genet,1989

2. Sensorineural deafness inherited as a tissue specific mitochondrial disorder;Jaber, L.; Shohat, M.; Bu, X.;_7 Med Genet,1992

3. Genetic aspects of antibiotic induced deafness: mitochondrial inheritance;Hu, D.N.; Qiu, W.Q.; Wu, B.T.;_7 Med Genet,1991

4. Mitochondrial ribosomal RNA mutation associated with both antibioticinduced and nonsyndromic deafness;Prezant, T.R.; Agapian, J.V.; Bohlman, M.C.;Nat Genet,1993

5. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity;Fischel-Ghodsian, N.; Prezant, T.R.; Bu, X.; Oztas, S.;Ant Otolaryngol,1993

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