Characterization of a Novel Cellular Defect in Patients with Phenotypic Homozygous Familial Hypercholesterolemia

AuthID
 P-00F-P0R
6
Author(s)
Norman, D
·
Sun, XM
·
Knight, BL
·
Naoumova, RP
·
Soutar, AK
Tipo de Documento
Article
Year published
1999
Publicado
in Journal of Clinical Investigation, ISSN: 0021-9738
Volume: 104, Número: 5, Páginas: 619-628
Indexing
Scopus®
Pubmed®
Publication Identifiers
Pubmed: 10487776
SCOPUS: 2-s2.0-0032728972
Source Identifiers
ISSN: 0021-9738
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