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XM_006508746
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Summary
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Body Atlas
Most Correlated Tissues
Whole blood
Monocyte of peripheral blood
Neutrophil of bone marrow
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Leukocyte (polymorphonuclear) of peripheral blood
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Literature
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A Case of Fetal Familial Hemophagocytic Lymphohistiocytosis Type 5 caused by STXBP2 Gene Mutation.
Secondary Leukemia in a Patient With EBV-HLH Carrying Heterozygous STXBP2 Variant.
Monogenic inflammatory bowel disease with STXBP2 mutations is not resolved by hematopoietic stem cel…
Syntaxin binding protein 2 in sertoli cells regulates spermatogonial stem cell maintenance through d…
Case Report: Characterizing the Role of the STXBP2-R190C Monoallelic Mutation Found in a Patient Wit…
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