Phenotypic expression of familial hypobetalipoproteinemia in three kindreds with mutations of apolipoprotein B gene

Journal of Lipid Research

Volumn 42, Issue 10, 2001, Pages 1552-1561

  Tarugi, Patrizia ^a   Lonardo, Amedeo ^b   Gabelli, Carlo ^c   Sala, Franca ^a   Ballarini, Giorgia ^a   Cortella, Irene ^c   Previato, Lorenzo ^c   Bertolini, Stefano ^d   Cordera, Renzo ^d   Calandra, Sebastiano ^a  

^a UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

^b Ospedale di Modena   (Italy)

^c UNIVERSITY OF PADOVA   (Italy)

^d UNIVERSITY OF GENOA   (Italy)

Author keywords

Carotid atherosclerosis; Fatty liver; Lipid malabsorption; Truncated apoBs

Indexed keywords

APOLIPOPROTEIN B;

ADULT; AGED; ALCOHOL CONSUMPTION; ARTICLE; ATHEROSCLEROSIS; CASE REPORT; CEREBROVASCULAR DISEASE; CONTROLLED STUDY; ENVIRONMENTAL FACTOR; EXON; FATTY LIVER; FEMALE; GENE DELETION; GENE EXPRESSION; HETEROZYGOTE; HUMAN; HYPOBETALIPOPROTEINEMIA; LIPID ABSORPTION; MALABSORPTION; MALE; NONSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; STEATORRHEA; STOP CODON;

ADULT; AGED; AMINO ACID SEQUENCE; APOLIPOPROTEINS B; BASE SEQUENCE; CENTRIFUGATION, DENSITY GRADIENT; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; HUMANS; LIPIDS; LIPOPROTEINS; LIVER; MALE; MUTATION; PEDIGREE; PHENOTYPE; TANGIER DISEASE;

EID: 0034763555     PISSN: 00222275     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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