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Lipoprotein(a) in homozygous familial hypercholesterolemia

Author
KRAFT, H. G1 ; LINGENHEL, A1 ; RAAL, F. J2 ; HOHENEGGER, M1 ; UTERMANN, G1
[1] Institute for Medical Biology and Human Genetics, University of Innsbruck, Innsbruck, Austria
[2] Department of Medicine, University of Witwatersrand, Johannesburg, South Africa
Source

Arteriosclerosis, thrombosis, and vascular biology. 2000, Vol 20, Num 2, pp 522-528 ; ref : 33 ref

CODEN
ATVBFA
ISSN
1079-5642
Scientific domain
Cardiology, blood circulation, phlebology
Publisher
Lippincott, Hagerstown, MD / Lippincott, Philadelphia, PA
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Déterminisme génétique Gène Homme Hypercholestérolémie Héréditaire Lipide Lipoprotéine LDL Lipoprotéine a Mutation Récepteur biologique Dyslipémie Hyperlipoprotéinémie Métabolisme pathologie
Keyword (en)
Genetic determinism Gene Human Hypercholesterolemia Hereditary Lipids Lipoprotein LDL Lipoprotein a Mutation Biological receptor Dyslipemia Hyperlipoproteinemia Metabolic diseases
Keyword (es)
Determinismo genético Gen Hombre Hipercolesterolemia Hereditario Lípido Lipoproteína LDL Lipoproteina a Mutación Receptor biológico Dislipemia Hiperlipoproteinemia Metabolismo patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22A Disorders of blood lipids. Hyperlipoproteinemia

Discipline
Metabolic diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
1263817

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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