1. Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family
    Yu-He Qi et al, 2017, Front. Genet. 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. RP1L1 and inherited photoreceptor disease: A review
    Nicole C.L. Noel et al, 2020, Survey of Ophthalmology CrossRef
  4. Occult Macular Dystrophy: a case report and major review
    Gracia Luoma-Overstreet et al, 2022, Ophthalmic Genetics CrossRef
  5. Research progress of RP1L1 gene in disease
    Jiali Liu et al, 2024, Gene CrossRef