| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8646176 | Gene Reports | 2018 | 25 Pages |
Abstract
In this study, we verified the association of (CCTTT)12 and VKC disease. Therefore, the concerned nucleotide change can be employed as an informative tool in determining the disease prognosis and detection of carriers, identification tests and elucidating the mechanism by which VKC develops.
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Genetics
Authors
Farzaneh Aali, Shahrbanou Parchami Barjui, Faranak Aali, Somaye Reiisi, Morteza Hashemzadeh Chaleshtori, Ali Salehi,