Prevalence and Clinical Features of the Mitochondrial m.1555A>G Mutation in Taiwanese Patients with Idiopathic Sensorineural Hearing Loss and Association of Haplogroup F with Low Penetrance in Three Families-Reference-Cited by-同舟云学术

Prevalence and Clinical Features of the Mitochondrial m.1555A>G Mutation in Taiwanese Patients with Idiopathic Sensorineural Hearing Loss and Association of Haplogroup F with Low Penetrance in Three Families

Published:2007-06 Issue:3 Volume:28 Page:332-342
ISSN:0196-0202
Container-title:Ear & Hearing
language:en
Short-container-title:

Author:

Wu Chen-Chi,Chiu Yu-Hsun,Chen Pei-Jer,Hsu Chuan-Jen

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Speech and Hearing,Otorhinolaryngology

Reference46 articles.

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2. Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.;Abe;European Journal of Human Genetics,1998

3. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness.;Bacino;Pharmacogenetics,1995

4. Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment.;Ballana;Biochemical and Biophysical Research Communications,2006

5. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.;Brown;American Journal of Human Genetics,1997

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