Cobalamin and inborn errors of cobalamin absorption and metabolism

Endocrinologist

Volumn 11, Issue 2, 2001, Pages 98-104

  Watkins, David ^a,d   Rosenblatt, David S ^a,b,c  

^a MCGILL UNIVERSITY   (Canada)

^b Department of Human Genetics ^*  (Canada)

^c MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

^d ROYAL VICTORIA HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

COBALAMIN; COBAMAMIDE; HOMOCYSTEINE; INTRINSIC FACTOR; MECOBALAMIN; METHIONINE; METHYLMALONIC ACID;

AMINO ACID DEFICIENCY; CLINICAL FEATURE; COENZYME; DRUG ABSORPTION; GENE MUTATION; HUMAN; HYPERHOMOCYSTEINEMIA; INBORN ERROR OF METABOLISM; METHYLMALONIC ACIDURIA; REVIEW; SYMPTOM; VITAMIN METABOLISM;

EID: 0035067124     PISSN: 10512144     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019616-200103000-00005     Document Type: Review

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