Genetic analysis of early onset familial coronary artery diseases.
- Published in:
- Archives of Medical Science - Atherosclerotic Diseases, 2019, v. 4, n. 1, p. e1, doi. 10.5114/amsad.2019.83149
- By:
- Publication type:
- Article
Works by Ghorbani, Mohammad Javad
Results: 4
1
2
A substitution mutation in LRP8 gene is significantly associated with susceptibility to familial myocardial infarction.
- Published in:
- ARYA Atherosclerosis, 2020, v. 16, n. 6, p. 301, doi. 10.22122/arya.v16i6.1797
- By:
- Publication type:
- Article
3
Update on a previously reported missense mutation: The c.1160 C>A mutation in the UGT1A1 gene result in Crigler–Najjar syndrome type 1.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
4
Analysis of HSP70-2 gene G1267A polymorphism in Helicobacter pylori infected patients.
- Published in:
- Journal of Mazandaran University of Medical Sciences (JMUMS), 2014, v. 23, p. 127
- By:
- Publication type:
- Article