| Bildiri Türü | Tebliğ/Bildiri | Bildiri Dili | İngilizce |
| Bildiri Alt Türü | |||
| Bildiri Niteliği | Web of Science Kapsamındaki Kongre/Sempozyum | ||
| DOI Numarası | 10.1007/s12031-012-9947-6 | ||
| Kongre Adı | |||
| Kongre Tarihi | / | ||
| Basıldığı Ülke | Basıldığı Şehir | ||
| Bildiri Linki | https://link.springer.com/article/10.1007/s12031-012-9947-6 | ||
| UAK Araştırma Alanları |
Tıbbi Biyoloji
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| Özet |
| Genetic risk factors are known to contribute to the etiology of multiple sclerosis (MS). Patients with familial Mediterranean fever (FMF) have susceptibility to develop MS. Mediterranean fever (MEFV) gene has already been identified as being responsible for FMF. The aim of this study was to explore the frequency of missense mutations of MEFV gene in a cohort of Turkish patients with MS. The study included 100 patients with MS and 160 healthy controls. Genomic DNA was isolated and genotyped using polymerase chain reaction and restriction fragment length polymorphism analyses for the five MEFV gene mutations (M694V, M680I, V726A, E148Q, and P369S). There were statistically significant differences of the MEFV gene mutation carrier rates and allele frequencies between MS patients and healthy controls (p = 0.0008, odds ratio (OR) 2.6, 95 % confidence interval (CI) 1.47–4.77 and p = 0.0002, OR 2.6 … |
| Anahtar Kelimeler |
| FMF | MEFV gene mutation | Multiple sclerosis |
| Atıf Sayıları | |
| Yöksis | 1 |
| Web of Science | 9 |
| Dergi Adı | JOURNAL OF MOLECULAR NEUROSCIENCE |
| Kısa Adı | J MOL NEUROSCI |
| Yayıncı | HUMANA PRESS INC |
| Açık Erişim | Hayır |
| ISSN | 0895-8696 |
| E-ISSN | 1559-1166 |
| Wos Quartile | Q3 |
| Scopus Quartile | Q1 |
| Tarandığı Indeksler | SCIE , Scopus |
| WoS Kategoriler | BIOCHEMISTRY & MOLECULAR BIOLOGY | NEUROSCIENCES |
| Scopus Kategoriler | MEDICINE (MISCELLANEOUS) | CELLULAR AND MOLECULAR NEUROSCIENCE |