Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

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

Volumn 95, Issue 6, 1998, Pages 3059-3064

  Leclerc, D ^a   Wilson, A ^a,c   Dumas, R ^a,c   Gafuik, C ^a,c   Song, D ^a   Watkins, D ^b   Heng, H H Q ^d   Rommens, J M ^d   Scherer, S W ^d   Rosenblatt, D S ^b,c   Gravel, R A ^a,c,e  

^a MONTREAL CHILDREN S HOSPITAL   (Canada)

^b ROYAL VICTORIA HOSPITAL   (Canada)

^c MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

^d HOSPITAL FOR SICK CHILDREN   (Canada)

^e RESEARCH INSTITUTE OF THE MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; HOMOCYSTEINE; METHIONINE SYNTHASE; OXIDOREDUCTASE;

ARTICLE; DNA SEQUENCE; ENZYME DEFICIENCY; GENE MAPPING; HOMOCYSTINURIA; HUMAN; HUMAN CELL; MOLECULAR CLONING; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE HOMOLOGY;

5-METHYLTETRAHYDROFOLATE-HOMOCYSTEINE S-METHYLTRANSFERASE; AMINO ACID SEQUENCE; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 5; CLONING, MOLECULAR; DNA, COMPLEMENTARY; ENZYME ACTIVATION; FERREDOXIN-NADP REDUCTASE; FLAVOPROTEINS; GENETIC COMPLEMENTATION TEST; HOMOCYSTINURIA; HUMANS; HYBRID CELLS; MALE; MOLECULAR SEQUENCE DATA; SEQUENCE ANALYSIS, DNA; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 13144282730     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.6.3059     Document Type: Article

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