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PloS one, ISSN 1932-6203, 07/2009, Volume 4, Issue 7, pp. e6138 - e6138
Journal Article
PloS one, ISSN 1932-6203, 2011, Volume 6, Issue 9, pp. e24220 - e24220
Journal Article
Nature genetics, ISSN 1061-4036, 06/2008, Volume 40, Issue 6, pp. 710 - 712
Journal Article
PloS one, ISSN 1932-6203, 08/2008, Volume 3, Issue 8, pp. e2986 - e2986
Background: Rare mutations of the low-density lipoprotein receptor gene (LDLR) cause familial hypercholesterolemia, which increases the risk for coronary... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Receptors, LDL - genetics | Oligonucleotide Array Sequence Analysis | Risk Assessment | Humans | Risk Factors | Cholesterol, LDL - drug effects | Chromosome Mapping | Random Allocation | Case-Control Studies | Genetic Variation | Cholesterol, LDL - genetics | Coronary Disease - prevention & control | Anticholesteremic Agents - therapeutic use | Coronary Disease - genetics | Cholesterol, LDL - blood | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 10 | Medical research | Hypercholesterolemia | Blood cholesterol | Low density lipoproteins | Genes | Medicine, Experimental | Genetic research | Genetics | Genetic aspects | Single nucleotide polymorphisms | Coronary heart disease | Risk factors | Lipoproteins (low density) | Risk | Lipids | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Gene polymorphism | Epidemiology | Consortia | Confidence intervals | Randomization | Population | Lipoprotein (low density) receptors | Children | Heart diseases | Statistical analysis | Mortality | Coronary artery | Health risks | Environmental health | Genetic diversity | Regression analysis | Metabolism | LDLR gene | Apolipoproteins | Coronary artery disease | Low density lipoprotein | Cholesterol | Studies | Genetic variance | Hospitals | Coronary vessels | Alleles | Biomarkers | Receptor density | Adults | Mutation | Polymorphism | Index Medicus
Journal Article
Nature (London), ISSN 1476-4687, 11/2007, Volume 450, Issue 7171, pp. 887 - 892
Journal Article
PloS one, ISSN 1932-6203, 08/2012, Volume 7, Issue 8, pp. e41730 - e41730
Journal Article
by Leone, Maurizio A and Barizzone, Nadia and Esposito, Federica and Lucenti, Ausiliatrice and Harbo, Hanne F and Goris, An and Kockum, Ingrid and Oturai, Annette Bang and Celius, Elisabeth Gulowsen and Mero, Inger L and Dubois, Bénédicte and Olsson, Tomas and Søndergaard, Helle Bach and Cusi, Daniele and Lupoli, Sara and Andreassen, Bettina Kulle and Barcellos, L and Booth, D and Comabella, M and Compston, A and D'Alfonso, Sandra and De Jager, P and Fontaine, B and Hafler, D and Haines, J and Hauser, S.L and Hawkins, C and Hemmer, B and Hillert, J and Ivinson, A and Martin, R and Martinelli Boneschi, F and McCauley, J.L and Oksenberg, J and Oturai, A and Patsopoulos, N and Pericak-Vance, M and Saarela, J and Sawcer, S and Spurkland, A and Stewart, G and Zipp, F and Myhr, Kjell-Morten and Guerini, Franca R and Naldi, Paola and Galimberti, Daniela and Scarpini, Elio and Bergamaschi, Roberto and Di Sapio, Antonella and Caputo, Domenico and Rosso, Gabriella and Cordera, Susanna and Cavalla, Paola and Cavallo, Roberto and Benedetti, Maria D and Salvetti, Marco and Capra, Ruggero and Ghezzi, Angelo and Annovazzi, Pietro and Coniglio, Gabriella and Liberatore, Giuseppe and Rodegher, Mariaemma and Moiola, Lucia and Colombo, Bruno and Radaelli, Marta and Rossi, Paolo and Martinelli, Vittorio and Comi, Giancarlo and Martinelli-Boneschi, Filippo and International Multiple Sclerosis G and PROGRESSO Group and Wellcome Trust Case Control Consortium 2 and International Multiple Sclerosis Genetics Consortium and PROGEMUS Group and the International Multiple Sclerosis Genetics Consortium and the PROGEMUS Group and the Wellcome Trust Case Control Consortium 2 and the PROGRESSO Group
PloS one, ISSN 1932-6203, 06/2013, Volume 8, Issue 6, pp. e64408 - e64408