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Identification of a mitochondrial 12S rRNA A1555G mutation causing aminoglycoside-induced deafness in a large Thai family Cover

Identification of a mitochondrial 12S rRNA A1555G mutation causing aminoglycoside-induced deafness in a large Thai family

Asian Biomedicine
Volume 9 (2015): Issue 2 (April 2015)
By: Pongsathorn Chaiyasap,  Chalurmpon Srichomthong,  Siraprapa Tongkobpetch,  Kanya Suphapeetiporn and  Vorasuk Shotelersuk  
Open Access
|Jan 2017

Authors

Pongsathorn Chaiyasap

Interdepartment of Biomedical Sciences, Faculty of Graduate School, Chulalongkorn University, Bangkok, Thailand

Chalurmpon Srichomthong

Center of Excellence for Medical Genetics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
Excellence Center for Medical Genetics, King Chulalongkorn Memorial Hospital, the Thai Red Cross, Bangkok, Thailand

Siraprapa Tongkobpetch

Center of Excellence for Medical Genetics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
Excellence Center for Medical Genetics, King Chulalongkorn Memorial Hospital, the Thai Red Cross, Bangkok, Thailand

Kanya Suphapeetiporn

kanya.su@chula.ac.th

Center of Excellence for Medical Genetics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
Excellence Center for Medical Genetics, King Chulalongkorn Memorial Hospital, the Thai Red Cross, Bangkok, Thailand

Vorasuk Shotelersuk

Center of Excellence for Medical Genetics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
Excellence Center for Medical Genetics, King Chulalongkorn Memorial Hospital, the Thai Red Cross, Bangkok, Thailand
DOI: https://doi.org/10.5372/1905-7415.0902.389 | Journal eISSN: 1875-855X | Journal ISSN: 1905-7415
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Language: English
Page range: 211 - 215
Published on: Jan 31, 2017
Published by: Chulalongkorn University
In partnership with: Paradigm Publishing Services
Publication frequency: 6 issues per year
Keywords:
Aminoglycoside,
deafness,
mitochondrial DNA,
MT-RNR1,
A1555G,
mutation analysis,
Thai
Related subjects:
Medicine,
Assistive professions, nursing,
Basic medical science,
Basic medical science, other,
Clinical medicine,
Clinical medicine, other

© 2017 Pongsathorn Chaiyasap, Chalurmpon Srichomthong, Siraprapa Tongkobpetch, Kanya Suphapeetiporn, Vorasuk Shotelersuk, published by Chulalongkorn University
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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