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Acta Oto-Laryngologica Volume 131, 2011 - Issue 9
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AUDIOLOGY

Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation

Meichao MenDepartment of Otolaryngology, Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha City, Hunan Province
,
Lu JiangDepartment of Otolaryngology, Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha City, Hunan Province
,
Honghan WangDepartment of Otolaryngology, Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha City, Hunan Province
,
Yalan Liu State Key Laboratory of Medical Genetics of China, Central South University, Changsha City, Hunan Province, China
,
Zhengmao Hu State Key Laboratory of Medical Genetics of China, Central South University, Changsha City, Hunan Province, China
,
Chufeng HeDepartment of Otolaryngology, Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha City, Hunan Province
&
Yong FengDepartment of Otolaryngology, Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha City, Hunan ProvinceCorrespondence[email protected]
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Pages 970-975 | Received 20 Jan 2011, Accepted 20 Mar 2011, Published online: 19 Apr 2011

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Yu Ding, Jianhang Leng & Jing Zheng. (2011) Critical reassessment of a five-generation Chinese family carrying deafness-associated mitochondrial 1555A>G mutation. Acta Oto-Laryngologica 131:11, pages 1239-1240.
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Articles from other publishers (3)

Rodrigo Tzovenos Starosta & Marwan Shinawi. (2022) Primary Mitochondrial Disorders in the Neonate. NeoReviews 23:12, pages e796-e812.
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Adebolajo A. Adeyemo, Odunayo Oluwatosin & Olayemi O. Omotade. (2016) Study of streptomycin-induced ototoxicity: protocol for a longitudinal study. SpringerPlus 5:1.
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Julia M. Barbarino, Tracy L. McGregor, Russ B. Altman & Teri E. Klein. (2016) PharmGKB summary. Pharmacogenetics and Genomics 26:12, pages 558-567.
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