SLC19A2 抗体
(Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
This gene encodes the 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. [provided by RefSeq, Jul 2008].
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Aliases for SLC19A2 抗体
solute carrier family 19 member 2 (Slc19a2) 抗体solute carrier family 19 member 2 (SLC19A2) 抗体
solute carrier family 19 (thiamine transporter), member 2 (slc19a2) 抗体
SLC19A2 抗体
TC1 抗体
THMD1 抗体
THT1 抗体
THTR1 抗体
TRMA 抗体
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