The Clinical and Audiologic Features of Hearing Loss Due to Mitochondrial Mutations: Response to Editor

被引：0
|
作者：
Yelverton, Joshua C. [1 ]
Dodson, Kelley M. [1 ]
Arnos, Kathleen [2 ]
Pandya, Arti [3 ]
机构：
[1] Virginia Commonwealth Univ Hlth Syst, Dept Otolaryngol Head & Neck Surg, Richmond, VA 23298 USA
[2] Gallaudet Univ, Dept Sci Technol & Math, Washington, DC 20002 USA
[3] Virginia Commonwealth Univ Hlth Syst, Dept Human & Mol Genet, Richmond, VA USA
来源：
OTOLARYNGOLOGY-HEAD AND NECK SURGERY | 2013年 / 149卷 / 05期
基金：
美国国家卫生研究院;
关键词：
D O I：
暂无
中图分类号：
R76 [耳鼻咽喉科学];
学科分类号：
100213 ;
摘要：
引用
收藏
页码：795 / 796
页数：4
相关论文
共 50 条
  • [31] Clinical Features and Hearing Outcomes of Sudden Sensorineural Hearing Loss in Diabetic Patients
    Ju, Yeo Rim
    Park, Hyoung-sik
    Lee, Min Young
    Jung, Jae Yun
    Choi, Ji Eun
    JOURNAL OF AUDIOLOGY AND OTOLOGY, 2021, 25 (01): : 27 - 35
  • [32] Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss
    Bae, Jae Woong
    Lee, Kyu Yup
    Choi, Soo Young
    Lee, Sang Heun
    Park, Hong-Joon
    Kim, Un-Kyung
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2008, 22 (02) : 175 - 180
  • [33] Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss
    Cortes, Nicolas Gutierrez
    Pertuiset, Claire
    Dumon, Elodie
    Boerlin, Marine
    Hebert-Chatelain, Etienne
    Pierron, Denis
    Feldmann, Delphine
    Jonard, Laurence
    Marlin, Sandrine
    Letellier, Thierry
    Rocher, Christophe
    HUMAN MUTATION, 2012, 33 (04) : 681 - 689
  • [34] Prevalence of mitochondrial DNA mutations in sporadic patients with nonsyndromic sensorineural hearing loss
    Jiang, Hua
    Chen, Jia
    Li, Ying
    Lin, Peng-Fang
    He, Jian-Guo
    Yang, Bei-Bei
    BRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGY, 2016, 82 (04) : 391 - 396
  • [35] Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation
    Kobayashi, K
    Oguchi, T
    Asamura, K
    Miyagawa, M
    Horai, S
    Abe, S
    Usami, S
    AURIS NASUS LARYNX, 2005, 32 (02) : 119 - 124
  • [36] Cardiomyopathies due to homoplasmic mitochondrial tRNA mutations: morphologic and molecular features
    Giordano, Carla
    Perli, Elena
    Orlandi, Maurizia
    Pisano, Annalinda
    Tuppen, Helen A.
    He, Langping
    Ierino, Rocco
    Petruzziello, Luciano
    Terzi, Amedeo
    Autore, Camillo
    Petrozza, Vincenzo
    Gallo, Pietro
    Taylor, Robert W.
    d'Amati, Giulia
    HUMAN PATHOLOGY, 2013, 44 (07) : 1262 - 1270
  • [37] Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma
    Mayr, Johannes A.
    Meierhofer, David
    Zimmermann, Franz
    Feichtinger, Rene
    Koegler, Christian
    Ratschek, Manfred
    Schmeller, Nikolaus
    Sperl, Wolfgang
    Kofler, Barbara
    CLINICAL CANCER RESEARCH, 2008, 14 (08) : 2270 - 2275
  • [38] Late postnatal onset of hearing loss due to GJB2 mutations
    Pagarkar, Waheeda
    Bitner-Glindzicz, Maria
    Knight, Jeffrey
    Sirimanna, Tony
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2006, 70 (06) : 1119 - 1124
  • [39] CLINICAL-FEATURES OF CISPLATIN VESTIBULOTOXICITY AND HEARING-LOSS
    KOBAYASHI, H
    OHASHI, N
    WATANABE, Y
    MIZUKOSHI, K
    ORL-JOURNAL FOR OTO-RHINO-LARYNGOLOGY AND ITS RELATED SPECIALTIES, 1987, 49 (02): : 67 - 72
  • [40] Clinical and genetic features of hearing loss in facioscapulohumeral muscular dystrophy
    Lutz, Katie L.
    Holte, Lenore
    Kliethermes, Stephanie A.
    Stephan, Carrie
    Mathews, Katherine D.
    NEUROLOGY, 2013, 81 (16) : 1374 - 1377
12345