Characterization of lpd (lipid defect): A novel mutation on mouse chromosome 16 associated with a defect in triglyceride metabolism

Human Molecular Genetics

Volumn 7, Issue 4, 1998, Pages 743-750

  Wen, Xiao Yan ^a,b,c   Bryce, Dawn M ^a   Breitman, Martin L ^a,b  

^a MOUNT SINAI HOSPITAL   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c UNIVERSITY HEALTH NETWORK   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

TRIACYLGLYCEROL;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; ATHEROGENESIS; CELL VACUOLE; CHROMOSOME 16; CONTROLLED STUDY; FATTY LIVER; GENE DUPLICATION; GENE INSERTION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; GENETIC LINKAGE; HOMOZYGOSITY; HYPERTRIGLYCERIDEMIA; LIPID METABOLISM; LIVER HISTOLOGY; MOLECULAR CLONING; MOUSE; NONHUMAN; PRIORITY JOURNAL; RISK FACTOR; SOUTHERN BLOTTING; TRANSGENIC MOUSE; TRIACYLGLYCEROL BLOOD LEVEL;

ANIMALS; BLOTTING, SOUTHERN; CHOLESTEROL; CHROMOSOME MAPPING; CLONING, MOLECULAR; DISEASE MODELS, ANIMAL; LIVER; MICE; MICE, TRANSGENIC; MULTIGENE FAMILY; MUTAGENESIS; MUTATION; TRIGLYCERIDES;

ANIMALIA; MUS MUSCULUS;

EID: 0031947502     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.4.743     Document Type: Article

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