Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry-Reference-Cited by-同舟云学术

Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry

Published:2016-05-26 Issue:1 Volume:17 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Alves Rogério Marins,da Silva Costa Sueli Matilde,do Amôr Divino Miranda Paulo Mauricio,Ramos Priscila Zonzini,Marconi Thiago Gibbin,Santos Oliveira Gisele,Castilho Arthur Menino,Sartorato Edi Lúcia

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP)

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-016-0303-5

Reference36 articles.

1. Morton CC. Genetics, genomics and gene discovery in the auditory system. Hum Mol Genet. 2002;11:1229–40.

2. Jacobs HT, Hutchin TP, Kappi T, et al. Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment. Eur J Hum Genet. 2005;13:26–33.

3. Zorov DB, Krasnikov BF, Kuzminova AE, et al. Mitochondria revisited. Alternative functions of mitochondria. Biosci Rep. 1997;17:507–20.

4. Fischel-Ghodsian N. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity. Am J Otolaryngol. 1993;14:399–403.

5. Wang CY, Kong QP, Yao YG, et al. mtDNA mutation C1494T, haplogroup A, and hearing loss in Chinese. Biochem Biophys Res Commun. 2006;348:712–5.

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