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Pathogenic variants in IMPG1 cause autosomal dominant and autosomal recessive retinitis pigmentosa

Olivier, G; Corton, M; Intartaglia, D; Verbakel, SK; Sergouniotis, PI; Le Meur, G; Dhaenens, CM; Naacke, H; Avila-Fernandez, A; Hoyng, CB; Klevering, J; Bocquet, B; Roubertie, A; Senechal, A; Banfi, S; Muller, A; Hamel, CL; Black, GC; Conte, I; Roosing, S; Zanlonghi, X; Ayuso, C; Meunier, I; Manes, G

Manes, G (corresponding author), Univ Montpellier, F-34000 Montpellier, France.

JOURNAL OF MEDICAL GENETICS, 2021; 58 (8): 570

Abstract

Background Inherited retinal disorders are a clinically and genetically heterogeneous group of conditions and a major cause of visual impairment. Comm......

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