Mitochondrial vitamin B12-binding proteins in patients with inborn errors of cobalamin metabolism

Author:

Moras E.,Hosack A.,Watkins D.,Rosenblatt D.S.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference33 articles.

1. Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism;Gravel;Proc. Natl. Acad. Sci. USA,1975

2. Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant;Willard;Am. J. Hum. Genet.,1978

3. Failure of lysosomal release of vitamin B12: a new complementation group causing methylmalonic aciduria (cblF);Watkins;Am. J. Hum. Genet.,1986

4. Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblG;Watkins;J. Clin. Invest.,1998

5. Complementation studies in the cblA class of inborn error of cobalamin metabolism: evidence for interallelic complementation and for a new complementation class (cblH);Watkins;J. Med. Genet.,2000

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