DFNB31 ELISA试剂盒
(Deafness, Autosomal Recessive 31 (DFNB31))
This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Mar 2010].
| Catalog no. | 产品 | 适用 | 宿主 / 克隆类型 | 应用 | 价格和交货时间 |
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| DFNB31 ELISA 试剂盒 | 人 | – |
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| DFNB31 ELISA 试剂盒 | 小鼠 | – |
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| DFNB31 ELISA 试剂盒 | 大鼠 | – |
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