Maternally inherited hearing loss is associated with the novel mitochondrial tRNASer(UCN) 7505T>C mutation in a Han Chinese family
- 31 May 2010
- journal article
- Published by Elsevier BV in Molecular Genetics and Metabolism
- Vol. 100 (1), 57-64
- https://doi.org/10.1016/j.ymgme.2010.01.008
Abstract
No abstract availableKeywords
Funding Information
- National Institute on Deafness and Other Communication Disorders (RO1DC05230, RO1DC07696)
- National Basic Research Priorities Program of China (2004CCA02200)
- Ministry of Science and Technology of Zhejiang Province (2007G50G2090026)
This publication has 42 references indexed in Scilit:
- Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutationMitochondrion, 2010
- Failures in Mitochondrial tRNA Met and tRNA Gln Metabolism Caused by the Novel 4401A>G Mutation Are Involved in Essential Hypertension in a Han Chinese FamilyHypertension, 2009
- Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese familiesPharmacogenetics and Genomics, 2008
- Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigreesGene, 2007
- Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNASer(UCN) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing lossBiochemical and Biophysical Research Communications, 2007
- Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing lossBiochemical and Biophysical Research Communications, 2007
- Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutationGene, 2007
- Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA MutationsAmerican Journal of Human Genetics, 2006
- Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese familiesBiochemical and Biophysical Research Communications, 2006
- Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASer(UCN) gene in a Japanese familyBiochemical and Biophysical Research Communications, 2005