Carnitine uptake defect: Frameshift mutations in the human plasmalemmal carnitine transporter gene

Biochemical and Biophysical Research Communications

Volumn 252, Issue 2, 1998, Pages 396-401

  Lamhonwah, Anne Marie ^a   Tein, Ingrid ^a  

^a UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CARNITINE; CARRIER PROTEIN; COMPLEMENTARY DNA; SODIUM ION;

AMINO ACID SEQUENCE; AMINO ACID TRANSPORT; ARTICLE; BRAIN DISEASE; CARDIOMYOPATHY; CASE REPORT; CELL MEMBRANE; CHROMOSOME 5Q; FAILURE TO THRIVE; FIBROBLAST; FRAMESHIFT MUTATION; GENE MAPPING; GENE SEQUENCE; GENETIC DISORDER; HUMAN; HUMAN CELL; INBORN ERROR OF METABOLISM; LYMPHOBLAST; MOLECULAR CLONING; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

EID: 0032544981     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1998.9679     Document Type: Article

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