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An apolipoprotein CII mutation CIILys→Thr' identified in patients with hyperlipidemia

Author
HEGELE, R. A; CONNELLY, P. W; MAGUIRE, G. F; HUFF, M. W; LEITER, L; WOLFE, B. M; EVANS, A. J; LITTLE, A
Univ. Toronto, St Michael's hosp., dep. medicine biochemistry, Toronto M5A 1B6, Canada
Source

Disease markers. 1991, Vol 9, Num 2, pp 73-80 ; ref : 12 ref

CODEN
DMARD3
ISSN
0278-0240
Scientific domain
General medicine general surgery
Publisher
IOS Press, Amsterdam / IOS Press, Berlin / IOS Press, Oxford
Publication country
Netherlands
Document type
Article
Language
English
Keyword (fr)
Biologie moléculaire Exploration Focalisation isoélectrique Génétique Homme Hyperlipoprotéinémie Lipide Mutation Réaction chaîne polymérase Séquence nucléotide Variant génétique apolipoprotéine C Métabolisme pathologie
Keyword (en)
Molecular biology Exploration Isoelectrical focusing Genetics Human Hyperlipoproteinemia Lipids Mutation Polymerase chain reaction Nucleotide sequence Genetic variant Metabolic diseases
Keyword (es)
Biología molecular Exploración Focalización isoeléctrica Genética Hombre Hiperlipoproteinemia Lípido Mutación Reacción cadena polimerasa Secuencia nucleótido Variante genética 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
5101967

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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