- Whole-exome sequencing analysis in a case of primary congenital glaucoma due to the partial uniparental isodisomy
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Zavarzadeh PG, Bonyadi M, Abedi Z
- KMID: 2535363
- Genomics Inform.
- 2022 Sep;20(3):e28.
- doi: 10.5808/gi.21044
We described a clinical, laboratory, and genetic presentation of a pathogenic variant of the CYP1B1 gene through a report of a case of primary congenital glaucoma and a trio analysis... -
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- Polymorphisms of Promoter Region of TNF-α Gene in Iranian Azeri Turkish Patients with Behçet's Disease
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Abdolmohammadi R, Bonyadi M
- KMID: 2417582
- J Korean Med Sci.
- 2017 Jan;32(1):33-37.
- doi: 10.3346/jkms.2017.32.1.33
Behçet’s disease (BD) is a complex chronic relapsing inflammatory disorder of unknown etiology. Alterations of the tumor necrosis factor (TNF) expression related to the polymorphic alleles of TNF gene may... -
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