Article

Allogeneic hematopoietic stem cell transplantation in a case of congenital sideroblastic anemia with SLC25A38 mutation

2024-01-31

Abstract excerpt

Congenital sideroblastic anemia (CSA) is a rare genetic disease. SLC25A38 encodes a member of the mitochondrial membrane carrier protein family. Mutations in SLC25A38 have been found to be an important cause of transfusion-dependent CSA. Evidence-based medical treatment guidelines for CSA remain lacking, and hematopoietic stem cell transplantation (HSCT) is currently the only proven curative therapy for this disea...

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Literature Corpus work: 56c5e8f8-c06f-5e28-b0b5-66b56a26eb57
DOI: 10.22541/au.170668122.21111241/v1

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