Mitochondrial mutations and hearing loss: Paradigm for mitochondrial genetics

被引:62
|
作者
Fischel-Ghodsian, N
机构
[1] Cedars Sinai Med Ctr, Ahmanson Dept Pediat, Steven Spielberg Pediat Res Ctr, Los Angeles, CA 90048 USA
[2] Univ Calif Los Angeles, Sch Med, Los Angeles, CA USA
关键词
D O I
10.1086/301695
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:15 / 19
页数:5
相关论文
共 50 条
  • [21] The Clinical and Audiologic Features of Hearing Loss Due to Mitochondrial Mutations: Response to Editor
    Yelverton, Joshua C.
    Dodson, Kelley M.
    Arnos, Kathleen
    Pandya, Arti
    OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2013, 149 (05) : 795 - 796
  • [22] 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
  • [23] 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
  • [24] Mitochondrial mutation associated with hearing loss
    Weitzman J.B.
    Genome Biology, 2 (1)
  • [25] Hearing loss in children with mitochondrial disorders
    Chennupati, Sri Kiran
    Levi, Jessica
    Loftus, Patricia
    Jornlin, Carly
    Morlet, Thierry
    O'Reilly, Robert C.
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2011, 75 (12) : 1519 - 1524
  • [26] Mitochondrial syndromic sensorineural hearing loss
    Forli, F.
    Passetti, S.
    Mancuso, M.
    Seccia, V.
    Siciliano, G.
    Nesti, C.
    Berrettini, S.
    BIOSCIENCE REPORTS, 2007, 27 (1-3) : 113 - 123
  • [27] Mitochondrial mutations associated with hearing and balance disorders
    Ibrahim, Iman
    Dominguez-Valentin, Mev
    Segal, Bernard
    Zeitouni, Anthony
    da Silva, Sabrina Daniela
    MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2018, 810 : 39 - 44
  • [28] Extended screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss
    Tomofumi Kato
    Yutaka Nishigaki
    Yoshihiro Noguchi
    Noriyuki Fuku
    Taku Ito
    Eri Mikami
    Ken Kitamura
    Masashi Tanaka
    Journal of Human Genetics, 2012, 57 : 772 - 775
  • [29] Extended screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss
    Kato, Tomofumi
    Nishigaki, Yutaka
    Noguchi, Yoshihiro
    Fuku, Noriyuki
    Ito, Taku
    Mikami, Eri
    Kitamura, Ken
    Tanaka, Masashi
    JOURNAL OF HUMAN GENETICS, 2012, 57 (12) : 772 - 775
  • [30] Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss
    Joo, Sun Young
    Jang, Seung Hyun
    Kim, Jung Ah
    Kim, Se Jin
    Kim, Bonggi
    Kim, Hye-Youn
    Choi, Jae Young
    Gee, Heon Yung
    Jung, Jinsei
    JOURNAL OF KOREAN MEDICAL SCIENCE, 2023, 38 (48)