1. Yokokura, Shunji, Wada, Yuko, Nakai, Shigeyasu, Tamai, Makoto, Noda, Tetsuo. . Targeted disruption of FSCN2 gene induces retinopathy in mice. In Investigative ophthalmology & visual science, 46, 2905-15. doi:. https://pubmed.ncbi.nlm.nih.gov/16043865/
2. Tubb, B E, Bardien-Kruger, S, Kashork, C D, Siciliano, M J, Bryan, J. . Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genes. In Genomics, 65, 146-56. doi:. https://pubmed.ncbi.nlm.nih.gov/10783262/
3. Liu, Xiang, Zhao, Mengmeng, Xie, Yi, Jin, Changzhu, Han, Fengchan. 2018. Null Mutation of the Fascin2 Gene by TALEN Leading to Progressive Hearing Loss and Retinal Degeneration in C57BL/6J Mice. In G3 (Bethesda, Md.), 8, 3221-3230. doi:10.1534/g3.118.200405. https://pubmed.ncbi.nlm.nih.gov/30082328/
4. Liu, Rongrong, Shang, Wenjing, Liu, Yingying, Song, Xicheng, Han, Fengchan. 2024. Inhibition of the ILK-AKT pathway by upregulation of PARVB contributes to the cochlear cell death in Fascin2 gene knockout mice. In Cell death discovery, 10, 89. doi:10.1038/s41420-024-01851-5. https://pubmed.ncbi.nlm.nih.gov/38374196/
5. Wada, Y, Abe, T, Takeshita, T, Yanashima, K, Tamai, M. . Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosa. In Investigative ophthalmology & visual science, 42, 2395-400. doi:. https://pubmed.ncbi.nlm.nih.gov/11527955/
6. Jin, Zi-Bing, Mandai, Michiko, Homma, Kohei, Nao-I, Nobuhisa, Takahashi, Masayo. 2008. Allelic copy number variation in FSCN2 detected using allele-specific genotyping and multiplex real-time PCRs. In Investigative ophthalmology & visual science, 49, 3799-805. doi:10.1167/iovs.07-1656. https://pubmed.ncbi.nlm.nih.gov/18450588/
7. Horák, Pavel, Knoll, Ales, Dvorák, Josef. . The retinal fascin gene 2 (FSCN2)--partial structural analysis and polymorphism detection in dogs with progressive retinal atrophy (PRA). In Journal of applied genetics, 47, 361-4. doi:. https://pubmed.ncbi.nlm.nih.gov/17132901/
8. Gamundi, María José, Hernan, Imma, Maseras, Miquel, Valverde, Diana, Carballo, Miguel. 2005. Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration. In Molecular vision, 11, 922-8. doi:. https://pubmed.ncbi.nlm.nih.gov/16280978/