Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke

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Název: Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke
Autoři: Jaworek, T., Durda, J.P., Engstrom, G., Ilinca, A., Smith, Jennifer A., Söderholm, M., Weir, D.R., Lindgren, Arne G., Kittner, S.J., Early Onset Stroke Genetics Consortium of the International Stroke Genetics Consortium (ISGC)
Přispěvatelé: Lund University, Faculty of Medicine, Department of Clinical Sciences, Malmö, Cardiovascular Research - Epidemiology, Lunds universitet, Medicinska fakulteten, Institutionen för kliniska vetenskaper, Malmö, Kardiovaskulär forskning - epidemiologi, Originator, Lund University, Profile areas and other strong research environments, Strategic research areas (SRA), EpiHealth: Epidemiology for Health, Lunds universitet, Profilområden och andra starka forskningsmiljöer, Strategiska forskningsområden (SFO), EpiHealth: Epidemiology for Health, Originator, Lund University, Faculty of Medicine, Department of Clinical Sciences, Lund, Section IV, Neurology, Lund, Clinical Neurogenetics, Lunds universitet, Medicinska fakulteten, Institutionen för kliniska vetenskaper, Lund, Sektion IV, Neurologi, Lund, Klinisk neurogenetik, Originator, Lund University, Faculty of Medicine, Department of Clinical Sciences, Lund, Section IV, Neurology, Lund, Clinical Stroke Research Group, Lunds universitet, Medicinska fakulteten, Institutionen för kliniska vetenskaper, Lund, Sektion IV, Neurologi, Lund, Klinisk strokeforskning, Originator, Lund University, Faculty of Medicine, Department of Clinical Sciences, Lund, Section IV, Neurology, Lund, Lunds universitet, Medicinska fakulteten, Institutionen för kliniska vetenskaper, Lund, Sektion IV, Neurologi, Lund, Originator
Zdroj: Neurology. 99(16):E1738-E1754
Témata: Medical and Health Sciences, Basic Medicine, Neurosciences, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Neurovetenskaper, Medical Genetics and Genomics (including Gene Therapy), Medicinsk genetik och genomik (Här ingår: Genterapi)
Přístupová URL adresa: https://doi.org/10.1212/WNL.0000000000201006
Databáze: SwePub
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ISSN:00283878
1526632X
DOI:10.1212/WNL.0000000000201006