Author:
Lerner-Ellis Jordan P,Tirone Jamie C,Pawelek Peter D,Doré Carole,Atkinson Janet L,Watkins David,Morel Chantal F,Fujiwara T Mary,Moras Emily,Hosack Angela R,Dunbar Gail V,Antonicka Hana,Forgetta Vince,Dobson C Melissa,Leclerc Daniel,Gravel Roy A,Shoubridge Eric A,Coulton James W,Lepage Pierre,Rommens Johanna M,Morgan Kenneth,Rosenblatt David S
Publisher
Springer Science and Business Media LLC
Reference29 articles.
1. Rosenblatt, D. & Fenton, W.A. Inherited disorders of folate and cobalamin transport and metabolism in The Metabolic & Molecular Bases of Inherited Disease Vol. 3, 3897–3933 (McGraw-Hill, New York, 2001).
2. Rosenblatt, D.S. et al. Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC). J. Inherit. Metab. Dis. 20, 528–538 (1997).
3. Atkinson, J. Genetic Mapping of Cobalamin C Deficiency: Linkage to Chromosome 1p32–34. Thesis. Univ. of Toronto, (2003).
4. Homocysteine in Health and Disease (eds. Carmel, R. & Jacobsen, D.W.) (Cambridge Univ. Press, Cambridge, 2001).
5. Andersson, H.C. & Shapira, E. Biochemical and clinical response to hydroxocobalamin versus cyanocobalamin treatment in patients with methylmalonic acidemia and homocystinuria (cblC). J. Pediatr. 132, 121–124 (1998).
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