Molecular Genetics of Gucy2d Gene among Patients with Leber Congenital Amaurosis Attending National Eye Center Kaduna
Farida Sagir Yaro, Yahaya Abdullahi Umar, Deborah Madi Dibal, Nkechi E. Egbe, Zahra’u Umar, Firdausi Aliyu, Samuel Adavba, Muhammad I. Tahir, Aliyu Adamu & Zakiya Mahmood · Asian Journal of Biotechnology and Genetic Engineering · 2023
Leber congenital amaurosis (LCA) is a clinically and genetically heterogeneous disease that presents with the autosomal recessive pattern of inheritance. There are about 19 genes responsible for the pathogenic cause of the disease, with mutations in a few of the genes recorded. T...
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Research Article