Molecular genetic characterization of Congolese patients with oculocutaneous albinism
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference21 articles.
1. Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family . Identification of a common TAG haplotype in the mutated P gene;Aquaron;J. Hum. Genet.,2007
2. Albinism in Africa: a medical and social emergency;Brilliant;Int Health,2015
3. African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism;Durham-Pierre;Nat. Genet.,1994
4. Children with Albinism in African Regions : Their Rights to ‘ Being ’ and ‘ Doing;Franklin,2018
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. GENOTYPIC SPECTRUM OF ALBINISM IN MALI;2024-03-07
2. Novel compound heterozygous mutations in OCA2 gene were identified in a Chinese family with oculocutaneous albinism;Molecular Genetics & Genomic Medicine;2023-10-26
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