Oculocutaneous albinism in a patient with an OCA2 variant: molecular and clinical insights
Authors
Mostafa Neissi
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
Language: English
Page range: 154 - 163
Published on: Jun 30, 2025
Published by: Chulalongkorn University
In partnership with: Paradigm Publishing Services
Publication frequency: 6 issues per year
Related subjects:
© 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.