Associated Papers
Biallelic loss-of-function variants in C19orf44 lead to retinal degeneration.
Hussain HMJ et al.
Journal of Medical Genetics, 2025
Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy.
Ehrenberg M et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2025
Select a paper to view details