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Volumn 93, Issue 5, 2003, Pages
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A splice mutation in a Syrian autosomal recessive hypercholesterolemia family causes a two-nucleotide deletion of mRNA.
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Author keywords
[No Author keywords available]
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Indexed keywords
ARH PROTEIN, HUMAN;
COMPLEMENTARY DNA;
MESSENGER RNA;
SIGNAL TRANSDUCING ADAPTOR PROTEIN;
VESICULAR TRANSPORT ADAPTOR PROTEIN;
ALTERNATIVE RNA SPLICING;
CELL CULTURE;
CHEMISTRY;
GENE DELETION;
GENETIC TRANSFECTION;
GENETICS;
HUMAN;
HYPERLIPOPROTEINEMIA TYPE 2;
MUTATION;
NOTE;
NUCLEOTIDE SEQUENCE;
RECESSIVE GENE;
SYRIAN ARAB REPUBLIC;
ADAPTOR PROTEINS, SIGNAL TRANSDUCING;
ADAPTOR PROTEINS, VESICULAR TRANSPORT;
ALTERNATIVE SPLICING;
BASE SEQUENCE;
DNA MUTATIONAL ANALYSIS;
DNA, COMPLEMENTARY;
GENES, RECESSIVE;
HUMANS;
HYPERLIPOPROTEINEMIA TYPE II;
MUTATION;
RNA, MESSENGER;
SEQUENCE DELETION;
SYRIA;
TRANSFECTION;
TUMOR CELLS, CULTURED;
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EID: 0141429979
PISSN: None
EISSN: 15244571
Source Type: Journal
DOI: 10.1161/01.res.0000089508.53350.70 Document Type: Note |
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Times cited : (6)
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References (0)
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