The molecular landscape of oculocutaneous albinism in India and its therapeutic implications

Author:

Kohli SudhaORCID,Saxena RenuORCID,Puri Ratna Dua,Bijarnia Mahay SunitaORCID,Pal Swasti,Dubey Sudhisha,Arora Veronica,Verma IshwarORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference48 articles.

1. OMIM®Online Mendelian Inheritance in Man. Johns Hopkins University, Baltimore, MD; 1985. Albinism, Oculocutaneous, Type IA; OCA1A. # 203100; 6/2/1986 [Updated 01/27/2021]. Available from: https://www.omim.org/entry/203100.

2. Summers CG, Albinism. In: Lambert SR, Lyons CJ, editors. Taylor and Hoyt’s pediatric ophthalmology and strabismus. 6th ed. USA: Elsevier Inc; 2022. 403–10.

3. Kromberg JGR, Kerr R. Oculocutaneous albinism in southern Africa: historical background, genetic, clinical and psychosocial issues. Afr J Disabil. 2022;11:877.

4. The Lancet Child Adolescent Health. Albinism: myths and reality. Lancet Child Adolesc Health. 2019;3:511.

5. Jeevan Trust. Raising awareness about albinism in India. India, 2016. Available from https://www.thebetterindia.com/50960/jeevan-trust-albinism-awareness/.

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