Lessons in biology from patients with inborn errors of vitamin B 12 metabolism

Biochimie

Volumn 95, Issue 5, 2013, Pages 1019-1022

  Watkins, David ^a   Rosenblatt, David S ^a  

^a MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

Author keywords

Cobalamin; Exome sequencing; Mendelian disorders; Vitamin B12

Indexed keywords

5 METHYLTETRAHYDROFOLIC ACID; COBAMAMIDE; CYANOCOBALAMIN; MECOBALAMIN; METHIONINE SYNTHASE; METHYLMALONYL COENZYME A MUTASE; PROPIONIC ACID; RECEPTOR; TRANSCOBALAMIN RECEPTOR; UNCLASSIFIED DRUG;

CBLC GENE; CBLD GENE; CBLF GENE; CELL TRANSPORT; FIBROBLAST; GENE; HUMAN; INBORN ERROR OF METABOLISM; LYSOSOME; REVIEW; VITAMIN METABOLISM;

5-METHYLTETRAHYDROFOLATE-HOMOCYSTEINE S-METHYLTRANSFERASE; FIBROBLASTS; HUMANS; METHYLMALONYL-COA MUTASE; MODELS, BIOLOGICAL; VITAMIN B 12;

EID: 84875823483     PISSN: 03009084     EISSN: 61831638     Source Type: Journal    
DOI: 10.1016/j.biochi.2013.01.013     Document Type: Review

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