Author:
Fleming Judith C.,Neufeld Ellis J.
Reference51 articles.
1. Abbourd, M.R., Alexander, D., and Najjar, S.S. (1985). Diabetes Mellitus, Thiamine-Dependent Megaloblastic Anemia, and Sensorineural Deafness Associated with Deficient Alpha-Ketoglutarate Dehydrogenase Activity. J. Pediatr., 107, 537–541.
2. Balamurugan, K. and Said, H.M. (2002). Functional Role of Specific Amino Acid Residues in Human Thiamine Transporter SLCI9A2: Mutational Analysis. Am. J. Physiol. Gastrointest. Liver Physiol., 283, G37–G43.
3. Banikazemi, M., Diaz, O.A., Vossough, P., Jalali, M., Desnick, R.I., and Gelb, B.D. (1999). Localization of the Thiamine-Responsive Megaloblastic Anemia Syndrome Locus to a 1.4-cM Region of 1q23. Mol. Genet. Metab., 66, 193–198.
4. Bappal, B., Nair, R., Shaikh, H., Al Khusaiby, S.M., and de Silva, V. (2001) Five Years Followup of Diabetes Mellitus in Two Siblings with Thiamine Responsive Megaloblastic Anemia. Indian Pediatr., 38, 1295–1298.
5. Barrett, T.G., Poulton, K., Baines, M., and McCowen, C (1997). Muscle Biochemistry in Thiamin-Responsive Anaemia. J. Inherit. Metab. Dis., 20, 404–406.