• English
    • Persian
  • Persian 
    • English
    • Persian
  • ورود
مشاهده آیتم 
  •   صفحه اصلی مخزن دانش
  • TBZMED Published Academics Works
  • Published Articles
  • مشاهده آیتم
  •   صفحه اصلی مخزن دانش
  • TBZMED Published Academics Works
  • Published Articles
  • مشاهده آیتم
JavaScript is disabled for your browser. Some features of this site may not work without it.

Is the frameshift codons 8/9 (+G) [FSC 8/9 (+G)] ?-thalassemia mutation, detected by the polymerase chain reaction-amplification refractory mutation system, really FSC 8/9 (+G)?

Thumbnail
تاریخ
2009
نویسنده
Haghi, M
Feizi, AAH
Feizi, MAH
Pouladi, N
Ba?ak, AN
Metadata
نمایش پرونده کامل آیتم
چکیده
There are several polymerase chain reaction (PCR)-based approaches for the analysis of known mutations. The PCR-amplification refractory mutation system (PCR-ARMS) is one of the best known and frequently used for the detection of ?-thalassemia (?-thal) mutations. However, there is an important point to be considered when searching for the frameshift codon (FSC) 8 (-AA) and FSC 8/9 (+G) mutations. Whereas the primer is specific for the FSC 8 mutation only, the primer for the FSC 8/9 mutation does not discriminate between the FSC 8/9 and FSC 8 mutations. Thus, the high number of FSC8/9 mutations reported in countries like India, Pakistan and some regions of Iran may be due to the use of the FSC 8/9 primer, without taking the FSC 8 mutation into account. It is thus advisable to test for FSC 8 before the FSC 8/9 mutation whenever PCR-ARMS is the method of investigation for these two mutations. Copyright é Informa Healthcare USA, Inc.
URI
http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54794
Collections
  • Published Articles

Related items

Showing items related by title, author, creator and subject.

  • Screening of OTOF mutations in Iran: A novel mutation and review 

    Mahdieh, N; Shirkavand, A; Rabbani, B; Tekin, M; Akbari, B; Akbari, MT; Zeinali, S (2012)
    Objective: Mutations in OTOF have been reported to cause nonsyndromic hearing loss in different populations. The purpose of this study is screening of OTOF mutations in Iranian population. Methods: Thirty-eight consanguineous ...
  • Spectrum MYBPC3 Gene Mutations in Patients with Hypertrophic Cardiomyopathy, Reporting Two Novel Mutations from North-West of Iran 

    Emrahi, L; Tabrizi, MT; Gharehsouran, J; Ardebili, SMM; Estiar, MA (2016)
    Background: Hypertrophic cardiomyopathy (HCM) is the leading cause of sudden cardiac death (SCD) in children and young adults and is the most frequent genetically determined cardiovascular disease following autosomal ...
  • Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness 

    Esmaeili, M; Bonyadi, M; Nejadkazem, M (2007)
    Objective: DFNB1 locus has been reported as a major cause of autosomal recessive non-syndromic hearing toss (ARNSHL) worldwide. 35delG and del(GJB6-D13S1830) are thought to be two common mutations in this Locus among ...

مخزن دانش دانشگاه علوم پزشکی تبریز در نرم افزار دی اسپیس، کپی رایت 2018 ©  
تماس با ما | Send Feedback
Theme by 
Atmire NV
 

 

مرور

همه مخزنجامعه ها و مجموعه هابراساس تاریخ انتشارنویسنده هاعنوانهاموضوعاین مجموعهبراساس تاریخ انتشارنویسنده هاعنوانهاموضوع

حساب من

ورودثبت نام

مخزن دانش دانشگاه علوم پزشکی تبریز در نرم افزار دی اسپیس، کپی رایت 2018 ©  
تماس با ما | Send Feedback
Theme by 
Atmire NV