Slc19a2: Cloning and Characterization of the Murine Thiamin Transporter cDNA and Genomic Sequence, the Orthologue of the Human TRMA Gene
- 30 June 2001
- journal article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 73 (2) , 149-159
- https://doi.org/10.1006/mgme.2001.3184
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafnessNature Genetics, 1999
- The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporterNature Genetics, 1999
- Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndromeNature Genetics, 1999
- Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblastsJournal of Clinical Investigation, 1999
- Further studies on erythrocyte thiamin transport and phosphorylation in seven patients with thiamin‐responsive megaloblastic anaemiaJournal of Inherited Metabolic Disease, 1994
- Thiamine transport by erythrocytes and ghosts in thiamine‐responsive megaloblastic anaemiaJournal of Inherited Metabolic Disease, 1991
- Thiamine-Dependent Beriberi in the “Thiamine-Responsive Anemia Syndrome”New England Journal of Medicine, 1984
- Thiamine responsive anaemia: a study of two further casesBritish Journal of Haematology, 1982
- Thiamine-responsive megaloblastic anemia, sensorineural deafness, and diabetes mellitus: A new syndrome?The Journal of Pediatrics, 1978
- Thiamine-responsive megaloblastic anemiaThe Journal of Pediatrics, 1969