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-Reference-Cited by-同舟云学术

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

Published:2019-04 Issue: Volume:283 Page:52-60
ISSN:0021-9150
Container-title:Atherosclerosis
language:en
Short-container-title:Atherosclerosis

Author:

Blanco-Vaca Francisco,Martin-Campos Jesús M.^ORCID,Beteta-Vicente Ángel,Canyelles Marina,Martínez Susana,Roig Rosa,Farré Núria,Julve Josep^ORCID,Tondo Mireia^ORCID

Funder

Instituto de Salud Carlos III

FEDER

Fundació la Marató de TV3

ISCIII

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

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5. Chylomicron retention disease: a description of a new mutation in a very rare disease;Ferreira;Pediatr. Gastroenterol. Hepatol. Nutr.,2018

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