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A novel genotyping technique for discriminating LVAS-associated high-frequency variants in SLC26A4 gene
An increasing number of biological and epidemiological evidence suggests that c.919-2A > G and c.2168A > G variants of solute carrier family 26, member 4 (SLC26A4) gene play a critical role in the development of large vestibular aqueduct syndrome (LVAS). In this study, we developed a rapid gen...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492351/ https://www.ncbi.nlm.nih.gov/pubmed/32930899 http://dx.doi.org/10.1186/s13568-020-01102-7 |