COS7 GlyT2 variants associated with hyperekplexia

NIAID Data Ecosystem2026-05-02 收录

神经遗传性疾病机制

功能蛋白质组学

数据链接：

https://www.omicsdi.org/dataset/pride/PXD061845 数据链接链接失效反馈

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资源简介：

Multiplexed LC-MS/MS analysis of heterologous cells expressing a new GlyT2 variant found in an infantile patient diagnosed with hyperekplexia.

创建时间：

2025-08-04

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根系微生物互作

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蛋白质相互作用鉴定

功能蛋白质组学

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