The familial chylomicronemia syndrome

Endocrinology and Metabolism Clinics of North America

Volumn 27, Issue 3, 1998, Pages 551-567

  Santamarina Fojo, S ^a  

^a NATIONAL HEART LUNG AND BLOOD INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN C2; LIPOPROTEIN LIPASE;

CLINICAL EXAMINATION; ENZYME DEFICIENCY; FAMILIAL DISEASE; GENE MUTATION; HUMAN; HYPERLIPOPROTEINEMIA TYPE 1; HYPERTRIGLYCERIDEMIA; PRIORITY JOURNAL; REVIEW; SYNDROME;

EID: 0031666919     PISSN: 08898529     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0889-8529(05)70025-6     Document Type: Article

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