Novel GUCY2D Splicing Variants in Kurdish Leber Congenital Amaurosis Patients in Iraq
The current study examines the single-nucleotide polymorphism of the GUCY2D gene in blind patients with inherited Leber congenital amaurosis (LCA) from a molecular, medical, and genetic perspective. The study involved 33 patients with blindness and 11 healthy controls in Erbil Province, Kurdistan R...
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| Principais autores: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Koya University
2026-06-01
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| Colecção: | ARO-The Scientific Journal of Koya University |
| Assuntos: | |
| Acesso em linha: | https://aro.koyauniversity.org/index.php/aro/article/view/2651 |
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