Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements

Proceedings of the National Academy of Sciences of the United States of America

Volumn 99, Issue 24, 2002, Pages 15554-15559

  Dobson, C Melissa ^a   Wai, Timothy ^b   Leclerc, Daniel ^c   Wilson, Aaron ^a   Wu, Xuchu ^a   Doré, Carole ^b   Hudson, Thomas ^b,c   Rosenblatt, David S ^b,c   Gravel, Roy A ^a  

^a UNIVERSITY OF CALGARY   (Canada)

^b MCGILL UNIVERSITY   (Canada)

^c MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; ADENOSINE TRIPHOSPHATASE; CARRIER PROTEIN; CYANOCOBALAMIN; METHIONINE SYNTHASE; METHYLMALONYL COENZYME A MUTASE; OXIDOREDUCTASE;

AMINO ACID SUBSTITUTION; ARTICLE; CBLA GENE; CHROMOSOME 4Q; COENZYME; GENE; GENE IDENTIFICATION; GENE LOCATION; GENE MUTATION; GENE REARRANGEMENT; GENE SEQUENCE; GENE STRUCTURE; GENETIC COMPLEMENTATION; GENETIC DISORDER; HUMAN; HUMAN GENOME; METHYLMALONIC ACIDEMIA; NONHUMAN; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; OPERON; PRIORITY JOURNAL; PROKARYOTE; PROTEIN DOMAIN; SEQUENCE ANALYSIS; SKELETAL MUSCLE; STOP CODON;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; BASE SEQUENCE; CELL LINE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 4; DNA MUTATIONAL ANALYSIS; FEMALE; FIBROBLASTS; GENES; GENETIC COMPLEMENTATION TEST; HETERODUPLEX ANALYSIS; HUMANS; INFANT; LIVER; MALE; METABOLISM, INBORN ERRORS; METHYLMALONIC ACID; METHYLMALONYL-COA MUTASE; MOLECULAR SEQUENCE DATA; MUSCLE, SKELETAL; MUTAGENESIS, INSERTIONAL; MUTATION, MISSENSE; ORGAN SPECIFICITY; POINT MUTATION; RNA SPLICE SITES; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION; SEQUENCE HOMOLOGY, AMINO ACID;

BACTERIA (MICROORGANISMS); INSERTION SEQUENCES; PROKARYOTA;

EID: 0037180440     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.242614799     Document Type: Article

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