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SLC25A38 is a member of the mitochondrial carrier family. Additionally we are shipping SLC25A38 Antibodies (20) and many more products for this protein.
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Given the tolerability of glycine and folate in humans, this study points to a potential novel treatment for SLC25A38 congenital sideroblastic anemia
This study findings reveal a novel role for appoptosin in neurological disorders with tau neuropathology, linking caspase-3 (show CASP3 Proteins)-mediated tau cleavage to synaptic dysfunction and behavioral/motor defects.
Letter/Case Report: novel frameshift mutation in SLC25A38 causing congenital sideroblastic anaemia.
Several missense mutations are found in SLC25A38 in a Chinese population with congenital sideroblastic anemia.
Compares and contrasts all the known human SLC25A (show SLC25A25 Proteins)* genes and includes functional information.
Mutations in the SLC25A38 gene cause severe, non-syndromic, microcytic/hypochromic sideroblastic anemia in many populations.
Twelve CSA (show ERCC8 Proteins) probands had biallelic mutations in SLC25A38
This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia.
solute carrier family 25, member 38
, solute carrier family 25 member 38