این سایت در حال حاضر پشتیبانی نمی شود و امکان دارد داده های نشریات بروز نباشند
Iranian Journal of Public Health، جلد ۳۲، شماره ۳، صفحات ۴۷-۵۳
عنوان فارسی
چکیده فارسی مقاله
کلیدواژه‌های فارسی مقاله
عنوان انگلیسی "Molecular Analysis of Iranian Patients with Duchenne/Becker Muscular Dystrophies"
چکیده انگلیسی مقاله Duchenne Muscular Dystrophy (DMD) and the milder allelic Becker Muscular Dystrophy (BMD) are X-linked disorders. Both DMD & BMD result from heterogenous mutation in the dystrophin gene and in about 65% of the cases one or more exons of the gene are deleted or duplicated. One third of cases arise from new mutation and the rest are familial. To analyze the prevalence of deletion in Iranian patients, a deletion screening was performed on group 18 exons of dystrophin gene. Deletions were detected in 56.8% of patients. Seventy four percent of deleted exons were located in the major hot spot region, whereas 26% were in the minor hot spot one. The most frequently deleted exons were exons 50, 48 & 47 16.2%, 16.2% & 12% respectively. No deletion was detected in exon 43. The intragenic RFLP analysis (pERT87-15/BamHI & pERT87-8/Taql) were carried out on DNA samples obtained from 22 Iranian unrelated families (196 males & females) showing DMD & BMD clinical symptoms, that 45% of them had informative patterns. The percentage of heterozygosity was 22.75% for BamHl intragenic RFLP, and 22.75% for Taql intragenic RFLP.
کلیدواژه‌های انگلیسی مقاله
نویسندگان مقاله s خردمند کیا | s kheradmand kia


dd فرهود | dd farhud


s زینالی | s zeinali


ar mowjoodi | ar mowjoodi


حسین نجم آبادی | h najmabadi


f پورفرزاد | f pourfarzad


p درخشنده | p derakhshandeh


نشانی اینترنتی http://ijph.tums.ac.ir/index.php/ijph/article/view/1954
فایل مقاله فایلی برای مقاله ذخیره نشده است
کد مقاله (doi)
زبان مقاله منتشر شده en
موضوعات مقاله منتشر شده
نوع مقاله منتشر شده Articles
برگشت به: صفحه اول پایگاه   |   نسخه مرتبط   |   نشریه مرتبط   |   فهرست نشریات