Identification ofP gene mutations in individuals with oculocutaneous albinism in sub-Saharan Africa
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference27 articles.
1. A "G" to "A" mutation at position -1 of a 5' splice site in a late infantile form of Tay-Sachs disease.
2. African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism
3. How sensitive is PCR-SSCP?
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1. Functional analysis of two mutation sites in the OCA2 gene;Scientific Reports;2024-06-26
2. Oculocutaneous Albinism (OCA) Type 1–5;Genetic Syndromes;2024
3. Molecular genetic characterization of Congolese patients with oculocutaneous albinism;European Journal of Medical Genetics;2022-11
4. Precise in vivo functional analysis of DNA variants with base editing using ACEofBASEs target prediction;eLife;2022-04-04
5. Oculocutaneous albinism: epidemiology, genetics, skin manifestation, and psychosocial issues;Archives of Dermatological Research;2022-02-25
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