1. A novel frameshift mutation in FRMD7 causes X-linked infantile nystagmus in a Chinese family
    Junjue Chen et al, 2019, BMC Medical Genetics CrossRef
  2. Dealing with Nystagmus
    Luis H. Ospina, 2018, Journal of Binocular Vision and Ocular Motility CrossRef
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    Fanfei Liu et al, 2023, Frontiers in Ophthalmology CrossRef
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    Aleksandr V. Apaev, 2021, Russian Pediatric Ophthalmology CrossRef
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    Yanghui Xiu et al, 2018, Molecular Medicine Reports CrossRef
  6. The Phenotypic Spectrum of Albinism
    Charlotte C. Kruijt et al, 2018, Ophthalmology CrossRef
  7. Truncated FRMD7 proteins in congenital Nystagmus: novel frameshift mutations and proteasomal pathway implications
    Yuqing Su et al, 2024, BMC Medical Genomics CrossRef
  8. A Disease-Causing FRMD7 Variant in a Chinese Family with Infantile Nystagmus
    Shan Wu et al, 2019, Journal of Molecular Neuroscience CrossRef
  9. FRMD7 Gene Alterations in a Pakistani Family Associated with Congenital Idiopathic Nystagmus
    Muhammad Waqar Arshad et al, 2023, Genes CrossRef
  10. Genotype-Phenotype Analysis and Mutation Spectrum in a Cohort of Chinese Patients With Congenital Nystagmus
    Xiao-Fang Wang et al, 2021, Frontiers in Cell and Developmental Biology CrossRef