1. Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family
    Yu-He Qi et al, 2017, Frontiers in Genetics CrossRef
  2. Novel homozygous loss-of-function mutations in RP1 and RP1L1 genes in retinitis pigmentosa patients
    Maan Abdullah Albarry et al, 2019, Ophthalmic Genetics CrossRef
  3. Research progress of RP1L1 gene in disease
    Jiali Liu et al, 2024, Gene CrossRef
  4. RP1L1 and inherited photoreceptor disease: A review
    Nicole C.L. Noel et al, 2020, Survey of Ophthalmology CrossRef
  5. Occult Macular Dystrophy: a case report and major review
    Gracia Luoma-Overstreet et al, 2022, Ophthalmic Genetics CrossRef