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SLC19A2 encodes a thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness.
AV276020; AW322295; DDA1; high affinity thiamine transporter; reduced folate carrier protein (RFC) like; Slc19a2; solute carrier family 19 (thiamine transporter), member 2; solute carrier family 19 member 2; TC1; Thiamine carrier 1; Thiamine transporter 1; THMD1; THT1; THTR1; ThTr-1; TRMA
100 µL
100 µL
100 µL
100 µL
100 µg
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50 µg
100 µL
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