Whole genome sequencing of an African American family highlights toll like receptor 6 variants in Kawasaki disease susceptibility

10.1371/journal.pone.0170977

محفوظ في:

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Kim J., Shimizu C., Kingsmore S.F., Veeraraghavan N., Levy E., Dos Santos A.M.R., Yang H., Flatley J., Hoang L.T., Hibberd M.L., Tremoulet A.H., Harismendy O., Ohno-Machado L., Burns J.C.
مؤلفون آخرون:	MICROBIOLOGY AND IMMUNOLOGY
التنسيق:	مقال
منشور في:	2019
الموضوعات:	interleukin 6 toll like receptor 6 transcriptome MEF2A protein, human myocyte enhancer factor 2 TLR6 protein, human African American Article child clinical article controlled study disease predisposition erythrocyte sedimentation rate family female gene frequency gene linkage disequilibrium genome-wide association study genotype heterozygosity homozygosity human male mucocutaneous lymph node syndrome pattern recognition quantitative trait locus signal transduction whole genome sequencing genetic predisposition genetics human genome single nucleotide polymorphism African Americans Female Gene Frequency Genetic Predisposition to Disease Genome, Human Genome-Wide Association Study Humans Male MEF2 Transcription Factors Mucocutaneous Lymph Node Syndrome Polymorphism, Single Nucleotide Quantitative Trait Loci Toll-Like Receptor 6
الوصول للمادة أونلاين:	https://scholarbank.nus.edu.sg/handle/10635/161532
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!

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