Human Genome Epidemiology Literature Finder
Rare Diseases
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Query Trace: Chylomicron Retention Disease[original query] |
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Molecular analysis of APOB, SAR1B, ANGPTL3, and MTTP in patients with primary hypocholesterolemia in a clinical laboratory setting: Evidence supporting polygenicity in mutation-negative patients. Atherosclerosis 2019 2 283 52-60. Blanco-Vaca Francisco, Martin-Campos Jesús M, Beteta-Vicente Ángel, Canyelles Marina, Martínez Susana, Roig Rosa, Farré Núria, Julve Josep, Tondo Mire |
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