Literature DB >> 10868237

Sensorineural hearing loss associated with the mitochondrial mutations.

S Usami1, S Abe, J Akita, H Shinkawa, W J Kimberling.   

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Year:  2000        PMID： 10868237     DOI： 10.1159/000059087

Source DB:  PubMed          Journal:  Adv Otorhinolaryngol        ISSN： 0065-3071


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  3 in total

1.  Patients with CDH23 mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS).

Authors:  Shin-ichi Usami; Maiko Miyagawa; Shin-ya Nishio; Hideaki Moteki; Yutaka Takumi; Mika Suzuki; Yoko Kitano; Satoshi Iwasaki
Journal:  Acta Otolaryngol       Date:  2012-04       Impact factor: 1.494

2.  Investigation of the A1555G mutation in mitochondrial DNA (MT-RNR1) in groups of Brazilian individuals with nonsyndromic deafness and normal-hearing.

Authors:  Karina Bezerra Salomão; Christiane Maria Ayo; Valter Augusto Della-Rosa
Journal:  Indian J Hum Genet       Date:  2013-01

3.  Cochlear Implantation From the Perspective of Genetic Background.

Authors:  Shin-Ichi Usami; Shin-Ya Nishio; Hideaki Moteki; Maiko Miyagawa; Hidekane Yoshimura
Journal:  Anat Rec (Hoboken)       Date:  2020-02-06       Impact factor: 2.064
  3 in total

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