1. Identification of a Novel Heterozygous Missense Mutation in theCACNA1FGene in a Chinese Family with Retinitis Pigmentosa by Next Generation Sequencing
   Qi Zhou et al, 2015, BioMed Research International CrossRef
2. Congenital Stationary Night Blindness: Clinical and Genetic Features
   Angela H. Kim et al, 2022, International Journal of Molecular Sciences CrossRef
3. The mGluR6 ligand-binding domain, but not the C-terminal domain, is required for synaptic localization in retinal ON-bipolar cells
   Melina A. Agosto et al, 2021, Journal of Biological Chemistry CrossRef
4. Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness
   Christina Zeitz et al, 2013, The American Journal of Human Genetics CrossRef
5. Retinoschisin Facilitates the Function of L-Type Voltage-Gated Calcium Channels
   Liheng Shi et al, 2017, Frontiers in Cellular Neuroscience CrossRef
6. Sequence features, structure, ligand interaction, and diseases in small leucine rich repeat proteoglycans
   Norio Matsushima et al, 2021, Journal of Cell Communication and Signaling CrossRef
7. Congenital stationary night blindness: An analysis and update of genotype–phenotype correlations and pathogenic mechanisms
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8. Leucine Rich Repeat Proteins: Sequences, Mutations, Structures and Diseases
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