Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations-Reference-Cited by-同舟云学术

Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations

Published:2006-08 Issue:2 Volume:79 Page:291-302
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Guan Min-Xin,Yan Qingfeng,Li Xiaoming,Bykhovskaya Yelena,Gallo-Teran Jaime,Hajek Petr,Umeda Noriko,Zhao Hui,Garrido Gema,Mengesha Emebet,Suzuki Tsutomu,Castillo Ignacio del,Peters Jennifer Lynne,Li Ronghua,Qian Yaping,Wang Xinjian,Ballana Ester,Shohat Mordechai,Lu Jianxin,Estivill Xavier,Watanabe Kimitsuna,Fischel-Ghodsian Nathan

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference53 articles.

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3. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness;Prezant;Nat Genet,1993

4. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycosides;Estivill;Am J Hum Genet,1998

5. Cosegregation of C-insertion at position 961 with A1555G mutation of mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss;Li;Am J Med Genet A,2004

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