Detalhe da pesquisa
1.
The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings.
Am J Hum Genet;
110(9): 1482-1495, 2023 09 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37652022
2.
SNPs at the APOA5 gene account for the strong association with hypertriglyceridaemia at the APOA5/A4/C3/A1 locus on chromosome 11q23 in the Northern Irish population.
Atherosclerosis;
185(2): 353-60, 2006 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16125709
3.
The LDLR variant T705I does not cause the typical phenotype of familial hypercholesterolaemia.
Atherosclerosis;
188(1): 218-9, 2006 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16735037
4.
Genetic screening of the LPL gene in hypertriglyceridaemic patients.
Atherosclerosis;
199(1): 187-92, 2008 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18068174