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المؤلفون: Chiea Chuen Khor, Peter W. M. Hermans, David Inwald, Enitan D. Carrol, Taco W. Kuijpers, Marieke Emonts, Victoria J. Wright, Chui Chin Lim, Kar Seng Sim, Sonia Davila, Ronald de Groot, Jan A. Hazelzet, Antonio Salas, Martin L. Hibberd, Willemijn B. Breunis, Simon Nadel, A. Binder, Federico Martinón-Torres, Werner Zenz, Michael Levin, Helen Betts
المساهمون: Paediatric Infectious Diseases / Rheumatology / Immunology, Paediatric Oncology, AII - Amsterdam institute for Infection and Immunity, Pediatrics
المصدر: Nature genetics, 42(9), 772-U63. Nature Publishing Group
Nature Genetics, 42, 9, pp. 772-6
Nature Genetics, 42(9), 772-776. Nature Publishing Group
Nature Genetics, 42(9), 772-U63. Nature Publishing Group
Nature Genetics, 42, 772-6مصطلحات موضوعية: Adult, Male, Adolescent, Genetic Linkage, Population, CHILDREN, HAPLOTYPE, Single-nucleotide polymorphism, Genome-wide association study, Complement factor I, Neisseria meningitidis, Biology, medicine.disease_cause, Meningococcal disease, Polymorphism, Single Nucleotide, COMPLEMENT FACTOR-H, Young Adult, Genetics, medicine, Humans, Genetic Predisposition to Disease, Child, education, SYSTEMIC MENINGOCOCCEMIA, RISK, education.field_of_study, Infant, Newborn, Infant, Middle Aged, MACULAR DEGENERATION, medicine.disease, Complement system, Pathogenesis and modulation of inflammation [N4i 1], Meningococcal Infections, Case-Control Studies, Child, Preschool, Complement Factor H, Factor H, Host-Pathogen Interactions, Immunology, 4G/5G PROMOTER POLYMORPHISM, Female, Infection and autoimmunity [NCMLS 1], PLASMINOGEN-ACTIVATOR-INHIBITOR-1 GENE, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46bb2cfc7f2b9eb24af91a9eda0bfac5Test
https://doi.org/10.1038/ng.640Test -
2دورية أكاديمية
المؤلفون: Davila, Sonia, Wright, Victoria J., Khor, Chiea Chuen, Sim, Kar Seng, Binder, Alexander, Breunis, Willemijn B., Inwald, David, Nadel, Simon, Betts, Helen, Carrol, Enitan D., de Groot, Ronald, Hermans, Peter W. M., Hazelzet, Jan, Emonts, Marieke, Lim, Chui Chin, Kuijpers, Taco W., Martinon-Torres, Federico, Salas, Antonio, Zenz, Werner, Levin, Michael, Hibberd, Martin L.
المصدر: Davila , S , Wright , V J , Khor , C C , Sim , K S , Binder , A , Breunis , W B , Inwald , D , Nadel , S , Betts , H , Carrol , E D , de Groot , R , Hermans , P W M , Hazelzet , J , Emonts , M , Lim , C C , Kuijpers , T W , Martinon-Torres , F , Salas , A , Zenz , W , Levin , M , Hibberd , M L & Int Meningococcal Genetics Consort ....
مصطلحات موضوعية: 4G/5G PROMOTER POLYMORPHISM, COMPLEMENT FACTOR-H, PLASMINOGEN-ACTIVATOR-INHIBITOR-1 GENE, SYSTEMIC MENINGOCOCCEMIA, MACULAR DEGENERATION, CHILDREN, HAPLOTYPE, RISK
الإتاحة: https://doi.org/10.1038/ng.640Test
https://hdl.handle.net/11370/4277e0de-b887-42f3-8843-27dd9ed2d812Test
https://research.rug.nl/en/publications/4277e0de-b887-42f3-8843-27dd9ed2d812Test