Analysis of MTHFR and MTRR gene polymorphisms in Iranian ventricular septal defect subjects
Ventricular septal defect (VSD) is one of the most common types of congenital heart defects (CHD). There are vivid multifactorial causes for VSD in which both genetic and environmental risk factors are consequential in the development of CHD. Methionine synthase reductase (MTRR) and methylenetetrahy...
محفوظ في:
المؤلفون الرئيسيون: | Pishva, Seyyed Reza, Vasudevan, Ramachandran, Etemad, Ali, Heidari, Farzad, Komara, Makanko, Ismail, Patimah, Othman, Fauziah, Karimi, Abdollah, Sabri, Mohammad Reza |
---|---|
التنسيق: | مقال |
اللغة: | English |
منشور في: |
MDPI
2013
|
الوصول للمادة أونلاين: | http://psasir.upm.edu.my/id/eprint/78040/1/78040.pdf http://psasir.upm.edu.my/id/eprint/78040/ https://www.mdpi.com/1422-0067/14/2/2739 |
الوسوم: |
إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
|
مواد مشابهة
-
Methylenetetrahydrofolate reductase and methionine synthase reductase gene polymorphisms in Iranian ventricular septal defect subjects
بواسطة: Pishva, Seyyed Reza
منشور في: (2013) -
Association of beta 2 adrenoceptor gene polymorphisms in Malaysian hypertensive subjects
بواسطة: Komara, Makanko, وآخرون
منشور في: (2014) -
Analysis of Gln223Agr polymorphism of leptin receptor gene in type II diabetic mellitus subjects among Malaysians
بواسطة: Etemad, Ali, وآخرون
منشور في: (2013) -
Genetic analysis of beta 2 adrenergic and Dopamine receptor gene polymorphisms in hypertensive subjects at Hospital Seremban, Malaysia
بواسطة: Komara, Makanko
منشور في: (2013) -
Mutational screening of exon 1 of smad7 in Malay patients
with ventricular septal defect
بواسطة: Hashim, Hashima
منشور في: (2015)