Title : Thiamine intestinal transport and related issues: recent aspects.

Pub. Date : 2000 Sep

PMID : 10964259






3 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 The saturable (specific) component is missing in patients of the rare disease known as thiamine-responsive megaloblastic anaemia (TRMA), producing a general disturbance of thiamine transport up to thiamine deficiency. Thiamine solute carrier family 19 member 2 Homo sapiens
2 The saturable (specific) component is missing in patients of the rare disease known as thiamine-responsive megaloblastic anaemia (TRMA), producing a general disturbance of thiamine transport up to thiamine deficiency. Thiamine solute carrier family 19 member 2 Homo sapiens
3 The saturable (specific) component is missing in patients of the rare disease known as thiamine-responsive megaloblastic anaemia (TRMA), producing a general disturbance of thiamine transport up to thiamine deficiency. Thiamine solute carrier family 19 member 2 Homo sapiens