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Volumn 38, Issue 2, 1997, Pages 191-205

The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes

Author keywords

familial LCAT deficiency; fish eye disease; genetics; HDL deficiency; human; lipoproteins; mutation

Indexed keywords

PHOSPHATIDYLCHOLINE STEROL ACYLTRANSFERASE;

EID: 0030933460     PISSN: 00222275     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (327)

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