Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population

OBJECTIVES: To investigate the cause of autosomal recessive non-syndromic hearing loss (ARNSHL) segregating in two consanguineous Iranian families. METHODS: Otologic and audiometric examinations were performed on affected members of each family. Genome-wide parametric multipoint linkage mapping usin...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Hildebrand, Michael S., Kahrizi, Kimia, Bromhead, Catherine J., Shearer, A. Eliot, Webster, Jennifer A., Khodaei, Hossein, Abtahi, Rezvan, Bazazzadegan, Niloofar, Babanejad, Mojgan, Nikzat, Nooshin, Kimberling, William J., Stephan, Dietrich, Huygen, Partick L.M., Bahlo, Melanie, Smith, Richard J.H., Najmabadi, Hossein
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3058627/
https://ncbi.nlm.nih.gov/pubmed/21250555
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados