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2. Ashraf, Tazeen, Vaina, Camelia, Giri, Dinesh, Ellard, Sian, Smithson, Sarah F. 2020. Expanding the phenotypic spectrum of IFT81: Associated ciliopathy syndrome. In American journal of medical genetics. Part A, 182, 2403-2408. doi:10.1002/ajmg.a.61781. https://pubmed.ncbi.nlm.nih.gov/32783357/
3. Tasaki, Koshi, Zhou, Zhuang, Ishida, Yamato, Katoh, Yohei, Nakayama, Kazuhisa. . Compound heterozygous IFT81 variations in a skeletal ciliopathy patient cause Bardet-Biedl syndrome-like ciliary defects. In Human molecular genetics, 32, 2887-2900. doi:10.1093/hmg/ddad112. https://pubmed.ncbi.nlm.nih.gov/37427975/
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5. Perrault, Isabelle, Halbritter, Jan, Porath, Jonathan D, Rozet, Jean-Michel, Hildebrandt, Friedhelm. 2015. IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype. In Journal of medical genetics, 52, 657-65. doi:10.1136/jmedgenet-2014-102838. https://pubmed.ncbi.nlm.nih.gov/26275418/
6. Duran, Ivan, Taylor, S Paige, Zhang, Wenjuan, Cohn, Daniel H, Krakow, Deborah. 2016. Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome. In Scientific reports, 6, 34232. doi:10.1038/srep34232. https://pubmed.ncbi.nlm.nih.gov/27666822/
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