[HTML][HTML] Gene Identification for the cblD Defect of Vitamin B12 Metabolism

D Coelho, T Suormala, M Stucki… - … England Journal of …, 2008 - Mass Medical Soc
Background Vitamin B12 (cobalamin) is an essential cofactor in several metabolic pathways.
Intracellular conversion of cobalamin to its two coenzymes, adenosylcobalamin in …

[引用][C] Gene Identification for the cblD Defect of Vitamin B12 Metabolism

D COELHO, T SUORMALA, M STUCKI… - The New England …, 2008 - pascal-francis.inist.fr
Gene Identification for the cblD Defect of Vitamin B12 Metabolism CNRS Inist Pascal-Francis
CNRS Pascal and Francis Bibliographic Databases Simple search Advanced search Search by …

Gene identification for the cblD defect of vitamin B12 metabolism.

D Coelho, T Suormala, M Stucki… - The New England …, 2008 - folia.unifr.ch
METHODS We studied seven patients with the cblD defect, and skin fibroblasts from each
were investigated in cell culture. Microcell-mediated chromosome transfer and refined …

Gene identification for the cblD defect of vitamin B12 metabolism.

D Coelho, T Suormala, M Stucki… - The New England …, 2008 - europepmc.org
Background Vitamin B12 (cobalamin) is an essential cofactor in several metabolic pathways.
Intracellular conversion of cobalamin to its two coenzymes, adenosylcobalamin in …

[PDF][PDF] Gene Identification for the cblD Defect of Vitamin B12 Metabolism

D Coelho, T Suormala, M Stucki, JP Lerner-Ellis… - N Engl J Med, 2008 - Citeseer
ResulTs The cblD gene was localized to human chromosome 2q23. 2, and a candidate
gene, designated MMADHC (methylmalonic aciduria, cblD type, and homocystinuria), was …

Gene identification for the cblD defect of vitamin B12 metabolism.

D Coelho, T Suormala, M Stucki, JP Lerner-Ellis… - The New England …, 2008 - sonar.ch
METHODS We studied seven patients with the cblD defect, and skin fibroblasts from each
were investigated in cell culture. Microcell-mediated chromosome transfer and refined …

Gene identification for the cblD defect of vitamin B12 metabolism

D Coelho, T Suormala, M Stucki… - The New England …, 2008 - edoc.unibas.ch
BACKGROUND: Vitamin B12 (cobalamin) is an essential cofactor in several metabolic
pathways. Intracellular conversion of cobalamin to its two coenzymes, adenosylcobalamin in …

[PDF][PDF] Gene Identification for the cblD Defect of Vitamin B12 Metabolism

D Coelho, T Suormala, M Stucki, JP Lerner-Ellis… - N Engl J Med, 2008 - academia.edu
ResulTs The cblD gene was localized to human chromosome 2q23. 2, and a candidate
gene, designated MMADHC (methylmalonic aciduria, cblD type, and homocystinuria), was …

[PDF][PDF] Gene Identification for the cblD Defect of Vitamin B12 Metabolism

D Coelho, T Suormala, M Stucki, JP Lerner-Ellis… - N Engl J Med, 2008 - core.ac.uk
ResulTs The cblD gene was localized to human chromosome 2q23. 2, and a candidate
gene, designated MMADHC (methylmalonic aciduria, cblD type, and homocystinuria), was …

Gene identification for the cblD defect of vitamin B12 metabolism

D Coelho, T Suormala, M Stucki… - The New England …, 2008 - pubmed.ncbi.nlm.nih.gov
Background Vitamin B12 (cobalamin) is an essential cofactor in several metabolic pathways.
Intracellular conversion of cobalamin to its two coenzymes, adenosylcobalamin in …