- A novel frameshift mutation in FRMD7 causes X-linked infantile nystagmus in a Chinese family
Junjue Chen et al, 2019, BMC Medical Genetics CrossRef - Dealing with Nystagmus
Luis H. Ospina, 2018, Journal of Binocular Vision and Ocular Motility CrossRef - X-linked FRMD7 gene mutation in idiopathic congenital nystagmus and its role in eye movement: A case report and literature review
Fanfei Liu et al, 2023, Frontiers in Ophthalmology CrossRef - Nystagmus: prevalence, classification, pathogenesis. (Literature review)
Aleksandr V. Apaev, 2021, Russian Pediatric Ophthalmology CrossRef - Identification of a novel idiopathic congenital nystagmus‑causing missense mutation, p.G296C, in the FRMD7 gene
Yanghui Xiu et al, 2018, Molecular Medicine Reports CrossRef - The Phenotypic Spectrum of Albinism
Charlotte C. Kruijt et al, 2018, Ophthalmology CrossRef - Truncated FRMD7 proteins in congenital Nystagmus: novel frameshift mutations and proteasomal pathway implications
Yuqing Su et al, 2024, BMC Medical Genomics CrossRef - A Disease-Causing FRMD7 Variant in a Chinese Family with Infantile Nystagmus
Shan Wu et al, 2019, Journal of Molecular Neuroscience CrossRef - FRMD7 Gene Alterations in a Pakistani Family Associated with Congenital Idiopathic Nystagmus
Muhammad Waqar Arshad et al, 2023, Genes CrossRef - 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