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Blood Cells, Molecules and Diseases, ISSN 1079-9796, 07/2018, Volume 71, pp. 39 - 44
Sideroblastic anemias are heterogeneous rare hematological disorders, representing diverse phenotypes. In this study, the genetic cause of congenital,... 
SLC25A38 | Congenital sideroblastic anemia | Microcytic hypochromic hemolytic anemia | Whole exome sequencing | Rare blood disorders | DIAGNOSIS | PYRIDOXINE | HEMATOLOGY | 5-AMINOLEVULINATE SYNTHASE | ALAS2 GENE
Journal Article
Clinical Case Reports, ISSN 2050-0904, 09/2018, Volume 6, Issue 9, pp. 1841 - 1844
The case of an infant girl with severe congenital sideroblastic anemia associated with a novel molecular defect in mitochondrial transporter SLC25A38 is... 
SLC25A38 | hematopoietic stem cell transplantation | sideroblastic anemia | Anemia | Stem cells
Journal Article
Journal Article
Oncology Letters, ISSN 1792-1074, 2014, Volume 7, Issue 5, pp. 1422 - 1426
SLC25A38 is a recently identified protein that belongs to the mitochondrial solute carrier family, SLC25. Previous studies have shown that it is a... 
Acute lymphoblastic leukemia | Molecular target | SLC25A38 protein | PATHWAYS | NOTCH1 | CONGENITAL SIDEROBLASTIC ANEMIA | CLASSIFICATION | 2ND REMISSION | MICRORNAS | molecular target | CARRIER | THERAPY | ONCOLOGY | acute lymphoblastic leukemia | MUTATIONS | GENE-EXPRESSION SIGNATURES
Journal Article
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