المؤلفون: Julien Niederhauser, François Spertini, Sven Bergmann, Goranka Tanackovic, Kim Ellefsen, Adriana Ransijn, Diana Marek, Stephanie Papin, Nathalie Isidor, Sébastien Jacquemont, Lucienne Poupon, Giuseppe Pantaleo, Jacques S. Beckmann

المصدر: Journal of Neuroinflammation, vol. 9, pp. 238
Journal of Neuroinflammation, Vol 9, Iss 1, p 238 (2012)
Journal of Neuroinflammation

مصطلحات موضوعية: Fragile X mental retardation 1 (FMR1) gene, Adult, Male, Ataxia, Aged, Alleles, Analysis of Variance, Case-Control Studies, Cytokines, Enzyme-Linked Immunosorbent Assay, Fragile X Mental Retardation Protein/genetics, Fragile X Syndrome/genetics, Fragile X Syndrome/metabolism, Humans, Interleukin-10/metabolism, Leukocytes, Mononuclear/metabolism, Middle Aged, Regression Analysis, Severity of Illness Index, Trinucleotide Repeat Expansion/genetics, medicine.medical_treatment, Immunology, Peripheral blood mononuclear cell, lcsh:RC346-429, Fragile X Mental Retardation Protein, Cellular and Molecular Neuroscience, Fragile X-associated tremor ataxia syndrome, medicine, Allele, lcsh:Neurology. Diseases of the nervous system, Genetics, Immune activation, Research, General Neuroscience, medicine.disease, FMR1, Interleukin-10, Fragile X syndrome, Cytokine, Neurology, Fragile X Syndrome, IL-10, Leukocytes, Mononuclear, medicine.symptom, Trinucleotide Repeat Expansion, Trinucleotide repeat expansion, Psychology, Fragile X-associated tremor/ataxia syndrome

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08fcb61d486f98cd4342c42702203805
https://doi.org/10.1186/1742-2094-9-238