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Study on the relationship between the pathogenic mutations of SLC26A4 and CT phenotypes of inner ear in patient with sensorineural hearing loss

To investigate the possible association of pathogenic mutations of SLC26A4 and computerized tomography (CT) phenotypes of inner ear, and explore the feasibility of using the method of gene sequence analysis. A total of 155 patients with bilateral hearing loss carrying SLC26A4 gene mutations were fur...

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Dades bibliogràfiques
Publicat a:Biosci Rep
Autors principals: Wu, Lihua, Liu, Yunliang, Wu, Jianman, Chen, Sheng, Tang, Shupin, Jiang, Yi, Dai, Pu
Format: Artigo
Idioma:Inglês
Publicat: Portland Press Ltd. 2019
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6430729/
https://ncbi.nlm.nih.gov/pubmed/30842343
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BSR20182241
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