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Oculocutaneous albinism in a patient with an OCA2 variant: molecular and clinical insights Cover

Oculocutaneous albinism in a patient with an OCA2 variant: molecular and clinical insights

Open Access
|Jun 2025

Authors

Mostafa Neissi

Iammostafaneissi@gmail.com

Department of Genetics, Khuzestan Science and Research Branch, Islamic Azad University, Ahvaz, Iran
Noor-Gene Genetic Laboratory, Ahvaz, Iran
Department of Genetics, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran

Sahar Kareem Al-Mozani

Department of Biology, University of Misan, Iraq

Ayoob Radhi Al-Zaalan

Department of Medical Lab Technology, College of Health and Medical Technology, Southern Technical University, Basrah, Iraq

Samaneh Sanavi Shiri

Amiralmomenin Hospital, Gerash, Iran

Motahareh Sheikh-Hosseini

Noor-Gene Genetic Laboratory, Ahvaz, Iran
Pediatric Cell and Gene Therapy Research Center, Tehran University of Medical Sciences, Tehran, Iran

Adnan Issa Al-Badran

Department of Biology, College of Science, University of Basrah, Basrah, Iraq

Elaheh Nekouei

Department of Biomedical and Clinical Science, Linköping University, Linköping, Sweden
DOI: https://doi.org/10.2478/abm-2025-0019 | Journal eISSN: 1875-855X | Journal ISSN: 1905-7415
Language: English
Page range: 154 - 163
Published on: Jun 30, 2025
In partnership with: Paradigm Publishing Services
Publication frequency: 6 issues per year

© 2025 Mostafa Neissi, Sahar Kareem Al-Mozani, Ayoob Radhi Al-Zaalan, Samaneh Sanavi Shiri, Motahareh Sheikh-Hosseini, Adnan Issa Al-Badran, Elaheh Nekouei, published by Chulalongkorn University
This work is licensed under the Creative Commons Attribution 4.0 License.