Some children with a familial hypercholesterolemia mutation may exhibit persistent low LDL levels.

Langslet, Gisle; Bogsrud, Martin P; Wium, Cecilie; Johansen, Dan; Svilaas, Arne; Holven, Kirsten B

Langslet, Gisle; Bogsrud, Martin P; Wium, Cecilie; Johansen, Dan; Svilaas, Arne; Holven, Kirsten B.

Affiliation

Langslet G; Norwegian National Advisory Unit on Familial Hypercholesterolemia, Oslo University, Hospital, Oslo, Norway; The Lipid Clinic, Oslo University Hospital, Oslo, Norway.
Bogsrud MP; Norwegian National Advisory Unit on Familial Hypercholesterolemia, Oslo University Hospital, Oslo, Norway; Unit for Cardiac and cardiovascular Genetics, Oslo University Hospital, Oslo, Norway.
Wium C; The Lipid Clinic, Oslo University Hospital, Oslo, Norway.
Johansen D; Norwegian National Advisory Unit on Familial Hypercholesterolemia, Oslo University Hospital, Oslo, Norway.
Svilaas A; The Lipid Clinic, Oslo University Hospital, Oslo, Norway.
Holven KB; Norwegian National Advisory Unit on Familial Hypercholesterolemia, Oslo University Hospital, Oslo, Norway; Department of Nutrition, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Oslo, Norway.

J Clin Lipidol ; 12(5): 1327-1328, 2018.

Article in En | MEDLINE | ID: mdl-30033003

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hyperlipoproteinemia Type II Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Child / Humans Country/Region as subject: Europa Language: En Journal: J Clin Lipidol Journal subject: BIOQUIMICA / METABOLISMO Year: 2018 Document type: Article Affiliation country: Noruega Country of publication: Estados Unidos

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