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Volumn 1, Issue 3, 1998, Pages 529-538
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A mutation in the lipoprotein lipase gene associated with hyperlipoproteinemia type I in mink: studies on lipid and lipase levels in heterozygotes.
a
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Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENTARY DNA;
LIPID;
LIPOPROTEIN LIPASE;
MESSENGER RNA;
ADIPOSE TISSUE;
AMINO ACID SEQUENCE;
AMINO ACID SUBSTITUTION;
ANIMAL;
ARTICLE;
BLOOD;
CHEMISTRY;
DNA SEQUENCE;
ENZYMOLOGY;
GENE;
GENETICS;
HEART MUSCLE;
HETEROZYGOTE;
HYPERLIPOPROTEINEMIA TYPE 1;
KIDNEY;
LUNG;
METABOLISM;
MINK;
MOLECULAR GENETICS;
MUSCLE;
NORTHERN BLOTTING;
NUCLEOTIDE SEQUENCE;
POINT MUTATION;
SEQUENCE ALIGNMENT;
SEQUENCE HOMOLOGY;
TISSUE DISTRIBUTION;
ADIPOSE TISSUE;
AMINO ACID SEQUENCE;
AMINO ACID SUBSTITUTION;
ANIMALS;
BASE SEQUENCE;
BLOTTING, NORTHERN;
DNA, COMPLEMENTARY;
GENES;
HETEROZYGOTE;
HYPERLIPOPROTEINEMIA TYPE I;
KIDNEY;
LIPIDS;
LIPOPROTEIN LIPASE;
LUNG;
MINK;
MOLECULAR SEQUENCE DATA;
MUSCLES;
MYOCARDIUM;
POINT MUTATION;
RNA, MESSENGER;
SEQUENCE ALIGNMENT;
SEQUENCE ANALYSIS, DNA;
SEQUENCE HOMOLOGY, AMINO ACID;
TISSUE DISTRIBUTION;
MLCS;
MLOWN;
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EID: 0032010086
PISSN: 11073756
EISSN: None
Source Type: Journal
DOI: 10.3892/ijmm.1.3.529 Document Type: Article |
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Times cited : (13)
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References (0)
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