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1.
Association of USF1 and APOA5 polymorphisms with familial combined hyperlipidemia in an Italian population.
Mol Cell Probes
; 29(1): 19-24, 2015 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-25308402
2.
An improved method on stimulated T-lymphocytes to functionally characterize novel and known LDLR mutations.
J Lipid Res
; 52(11): 2095-100, 2011 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-21865347
3.
The novel variant p.Ser465Leu in the PCSK9 gene does not account for the decreased LDLR activity in members of a FH family.
Clin Chem Lab Med
; 52(8): e175-8, 2014 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-24607922
4.
Identification and functional characterization of LDLR mutations in familial hypercholesterolemia patients from Southern Italy.
Atherosclerosis
; 210(2): 493-6, 2010 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-20045108
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