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

BACKGROUND: Mutations of mitochondrial DNA were described into two genes: The mitochondrially encoded 12S RNA (MT-RNR1) and the mitochondrially encoded tRNA serine(ucn) (MT-TS1). The A1555G mutation in MT-RNR1 gene is a frequent cause of deafness in different countries. AIM: The aim of this work was...

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Detalles Bibliográficos
Autores principales: Salomão, Karina Bezerra, Ayo, Christiane Maria, Della-Rosa, Valter Augusto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3722630/
https://www.ncbi.nlm.nih.gov/pubmed/23901193
http://dx.doi.org/10.4103/0971-6866.112888

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3722630/
https://www.ncbi.nlm.nih.gov/pubmed/23901193
http://dx.doi.org/10.4103/0971-6866.112888

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