Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness
Nature Genetics1999Vol. 22(3), pp. 300–304
Citations Over TimeTop 10% of 1999 papers
Valentina Labay, Tal Raz, Dana Baron, Hanna Mandel, Hawys Williams, Timothy Barrett, Raymonde Szargel, Louise McDonald, Adel Shalata, Kazuto Nosaka, Simon G. Gregory, Nadine Cohen
Related Papers
- → Thiamine Withdrawal Can Lead to Diabetic Ketoacidosis in Thiamine Responsive Megaloblastic Anemia: Report of Two Siblings(2008)24 cited
- → Mice That Are Congenic for the char2 Locus Are Susceptible to Malaria(2002)23 cited
- → Beta cell function and clinical course in three siblings with thiamine-responsive megaloblastic anemia (TRMA) treated with thiamine supplementation(2017)12 cited
- → Molecular Cloning of the Critical Region for Glomerulopathy with Fibronectin Deposits (GFND) and Evaluation of Candidate Genes(2000)13 cited
- Resolving the molecular basis of human malformation syndromes(2005)