Dstyk mutation leads to congenital scoliosis-like vertebral malformations in zebrafish via dysregulated mTORC1/TFEB pathway
Abstract Congenital scoliosis (CS) is a complex genetic disorder characterized by vertebral malformations. The precise etiology of CS is not fully defined. Here, we identify that mutation in dual serine/threonine and tyrosine protein kinase ( dstyk ) lead to CS-like vertebral malformations in zebraf...
Saved in:
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
格式: | Artigo |
语言: | 英语 |
出版: |
2020
|
在线阅读: | https://doi.org/10.1038/s41467-019-14169-z https://www.nature.com/articles/s41467-019-14169-z.pdf |
标签: |
添加标签
没有标签, 成为第一个标记此记录!
|