A new mutation in the human lipoprotein lipase gene causing familial hyperchylomicronaemia

Journal of Clinical Pathology - Molecular Pathology

Volumn 50, Issue 4, 1997, Pages 221-223

  Anwar, R ^a   Puntis, J W L ^a   Markham, A F ^a  

^a UNIVERSITY OF LEEDS   (United Kingdom)

Author keywords

DNA mutation; Hyperchylomicronaemia; Lipoprotein lipase

Indexed keywords

FATTY ACID; LIPOPROTEIN LIPASE; TRIACYLGLYCEROL;

AMINO TERMINAL SEQUENCE; ARTICLE; CASE REPORT; CELL MATURATION; ENZYME DEFICIENCY; ENZYME REGULATION; FEMALE; HOMOZYGOSITY; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERLIPOPROTEINEMIA TYPE 1; LIPID METABOLISM; MOLECULAR BIOLOGY; PRIORITY JOURNAL; PROTEIN DOMAIN; SCHOOL CHILD;

EID: 0030717658     PISSN: 13668714     EISSN: None     Source Type: Journal    
DOI: 10.1136/mp.50.4.221     Document Type: Article

References (9)

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