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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...

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Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: 2010
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3058627/
https://ncbi.nlm.nih.gov/pubmed/21250555
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