QuickView for STXBP2;jsessionid=6A2F860C0AF7E76917126C1637AED0D3;jsessionid=28811BBBE4FE655BF9A5D9956FC6B353;jsessionid=21E3E40A90CA0EE8032000F5C5DE21BA;jsessionid=EE8F5A5ACBF9CF4D50B343410EDE0819;jsessionid=436B75CDD631E4438E48177773EA83E2 (gene)

1. A Case of Fetal Familial Hemophagocytic Lymphohistiocytosis Type 5 caused by STXBP2 Gene Mutation.
2. Secondary Leukemia in a Patient With EBV-HLH Carrying Heterozygous STXBP2 Variant.
3. Monogenic inflammatory bowel disease with STXBP2 mutations is not resolved by hematopoietic stem cel…
4. Syntaxin binding protein 2 in sertoli cells regulates spermatogonial stem cell maintenance through d…
5. Case Report: Characterizing the Role of the STXBP2-R190C Monoallelic Mutation Found in a Patient Wit…

There were no clinical trials for STXBP2;jsessionid=6A2F860C0AF7E76917126C1637AED0D3;jsessionid=28811BBBE4FE655BF9A5D9956FC6B353;jsessionid=21E3E40A90CA0EE8032000F5C5DE21BA;jsessionid=EE8F5A5ACBF9CF4D50B343410EDE0819;jsessionid=436B75CDD631E4438E48177773EA83E2