SLC19A2: Proteins and Enzymes
SLC19A2 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.
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2 results for "SLC19A2 Proteins and Enzymes" in Products
2 results for "SLC19A2 Proteins and Enzymes" in Products
SLC19A2: Proteins and Enzymes
SLC19A2 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.
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| Applications: | WB, ELISA, MA, AP |
| Applications: | AC |