Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation.
第一作者:
Elif,Everest
第一单位:
Department of Molecular Biology and Genetics, Faculty of Science and Letters, Istanbul Technical University, Maslak, Istanbul, Turkey.
作者:
医学主题词
等位基因(Alleles);基因连锁(Genetic Linkage);疾病遗传易感性(Genetic Predisposition to Disease);遗传变异(Genetic Variation);人类(Humans);多发性硬化(Multiple Sclerosis);系谱(Pedigree)
DOI
10.1038/s41598-022-21484-x
PMID
36216875
发布时间
2024-11-16
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Scientific reports
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