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المؤلفون: Claudia Mischung, Elisabeth Steinhagen-Thiessen, Thomas Bobbert, Frieda Bardey, Ursula Kassner, Ilja Demuth, Johannes Helmuth, Thomas Grenkowitz, Lorenz Rieck, Joachim Spranger, Lars Bertram
المصدر: Clinical Genetics
مصطلحات موضوعية: Male, 0301 basic medicine, Multifactorial Inheritance, medicine.medical_specialty, Genotype, Apolipoprotein B, Single-nucleotide polymorphism, Familial hypercholesterolemia, 030105 genetics & heredity, medicine.disease_cause, Polymorphism, Single Nucleotide, Gastroenterology, Hyperlipoproteinemia Type II, 03 medical and health sciences, Risk Factors, Internal medicine, Genetics, medicine, Humans, Genetic variability, Genetics (clinical), low-density lipoprotein cholesterol, Mutation, familial hypercholesterolemia, biology, business.industry, PCSK9, Cholesterol, LDL, Middle Aged, medicine.disease, 030104 developmental biology, Receptors, LDL, Cardiovascular Diseases, Apolipoprotein B-100, LDL receptor, biology.protein, Kexin, Female, lipids (amino acids, peptides, and proteins), Proprotein Convertase 9, business, 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d61975a9c23fcdd37c16d39d6e2b30b2Test
https://doi.org/10.1111/cge.13826Test -
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المؤلفون: Ilja Demuth, Lars Bertram, E. Steinhagen-Thiessen, Thomas Bobbert, Johannes Helmuth, Claudia Mischung, Thomas Grenkowitz, Ursula Kassner, Joachim Spranger, Frieda Bardey, Lorenz Rieck
مصطلحات موضوعية: German, Genetics, business.industry, Mutation (genetic algorithm), language, Medicine, Familial hypercholesterolemia, business, medicine.disease, language.human_language
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eab2223a1c123723fb268221ebc4387eTest
https://doi.org/10.1111/cge.13826/v3/response1Test -
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