QuickView for STXBP2;jsessionid=6A2F860C0AF7E76917126C1637AED0D3;jsessionid=4933ED8D2DC6DAD2321DDD4A9E940EF1;jsessionid=DCD54EEB60B292297E05EFE86203F091;jsessionid=1B70E9FCEA14E09046592AE14931A490;jsessionid=E3F07EAADC93926286BC213390C094D1 (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=4933ED8D2DC6DAD2321DDD4A9E940EF1;jsessionid=DCD54EEB60B292297E05EFE86203F091;jsessionid=1B70E9FCEA14E09046592AE14931A490;jsessionid=E3F07EAADC93926286BC213390C094D1