<a name="home"></a>Prevalence of the A1555G (12S rRNA) and tRNA Ser(UCN) mitochondrial mutations in hearing-impaired Brazilian patients

<a name="home"></a>Prevalence of the A1555G (12S rRNA) and tRNA Ser(UCN) mitochondrial mutations in hearing-impaired Brazilian patients

Mitochondrial mutations are responsible for at least 1% of the cases of hereditary deafness, but the contribution of each mutation has not yet been defined in African-derived or native American genetic backgrounds. A total of 203 unselected hearing-impaired patients were screened for the presence of...

Full description

Bibliographic Details
Main Authors: R.S. Abreu-Silva, K. Lezirovitz, M.C.C. Braga, M. Spinelli, S. Pirana, V.A. Della-Rosa, P.A. Otto, R.C. Mingroni-Netto
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2006-02-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Mitochondrial DNA
Hearing impairment
A1555G mutation
tRNA Ser(UCN) mutations
European- and African- Brazilian patients
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2006000200008&lng=en&tlng=en

Similar Items

Similar Items