A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family

BACKGROUND: The genetic basis of autosomal dominant nonsyndromic hearing loss is complex. Genetic factors are responsible for approximately 50% of cases with congenital hearing loss. However, no previous studies have documented the clinical phenotype and genetic basis of autosomal dominant nonsyndro...

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Bibliografiset tiedot
Päätekijät: Bai, Haihua, Yang, Xukui, Temuribagen, Guilan, Suyalatu, Narisu, Narisu, Wu, Huiguang, Chen, Yujie, Liu, Yangjian, Wu, Qizhu
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2014
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3994966/
https://ncbi.nlm.nih.gov/pubmed/25008054
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-15-34
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