Long-term follow up of patients with transcobalamin II deficiency.

Author:

Monagle P T,Tauro G P

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference7 articles.

1. Hereditary abnormal transcobalamin II previously diagnosed as congenital dihydrofolate reductase deficiency;Hoffbrand, A.V.; Tripp, E.; Jackson, B.; Luck, W.;N Engl J Med,1984

2. Transcobalamin II deficiency: long term follow up of two cases;Arrabel, M.C.; Villegas, A.; Mariscal, E.;Acta Haematol,1988

3. Transcobalamin II case report and review of the literature;Kaikor, Y.; Wadsworth, L.; Hall, C.; Rogers, P.;Eur J Pediatr,1991

4. Congenital transcobalamin II deficiency presenting atypically with a low serum cobalamin level: studies demonstrating the coexistence of a circulating transcobalamin;Carmel, R.; Ravindranath, Y.,1984

5. Inherited lack of transcobalamin II in serum and megaloblastic anaemia: a further patient;Burman, J.F.; Mollin, D.L.; Sourial, N.A.; Sladder, R.A.;BrJt Haematol,1979

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