An interactive human PROS1 variants database provides novel insights into the genetics and phenotypes of inherited protein S deficiency

database[Title] 2026-04-17

Summary:

CONCLUSION: This database provides a valuable resource for retrieving pathogenic PROS1 variants and associated clinical data, enhancing our understanding of thrombotic risk in PSD and facilitating precision medicine for PSD.

Link:

https://pubmed.ncbi.nlm.nih.gov/41967715/?utm_source=Other&utm_medium=rss&utm_campaign=pubmed-2&utm_content=12QQbiNmM99eUQGIX1JjHIKcROC1Vzv4sOS-2S_LNI19uG_Yrk&fc=20220129225649&ff=20260417082646&v=2.19.0.post6+133c1fe

From feeds:

📚BioDBS Bibliography » database[Title]

Tags:

Authors:

Zepeng Hou, Fangni Liu, Shixia Dong, Yiming Guo, Xiaowei Yu, Li-Jiezhuo Ai, Mingshuo Zhang, Jingxuan Kang, Bo Jiang, Yanyan Dong, Meng Zhao, Jiahui Pan, Shujuan Zhang, Wenran Zhao, Wei Wang, Dapeng Hao, Guomin Shen

Date tagged:

04/17/2026, 08:33

Date published:

04/12/2026, 06:00