1. Furtado, Milena B, Merriner, D Jo, Berger, Silke, Jamsai, Duangporn, O'Bryan, Moira K. 2017. Mutations in the Katnb1 gene cause left-right asymmetry and heart defects. In Developmental dynamics : an official publication of the American Association of Anatomists, 246, 1027-1035. doi:10.1002/dvdy.24564. https://pubmed.ncbi.nlm.nih.gov/28791777/
2. O'Donnell, L, McLachlan, R I, Merriner, D Jo, O'Bryan, M K, Jamsai, D. 2014. KATNB1 in the human testis and its genetic variants in fertile and oligoasthenoteratozoospermic infertile men. In Andrology, 2, 884-91. doi:10.1111/andr.276. https://pubmed.ncbi.nlm.nih.gov/25280067/
3. Hu, Wen F, Pomp, Oz, Ben-Omran, Tawfeg, Reversade, Bruno, Walsh, Christopher A. . Katanin p80 regulates human cortical development by limiting centriole and cilia number. In Neuron, 84, 1240-57. doi:10.1016/j.neuron.2014.12.017. https://pubmed.ncbi.nlm.nih.gov/25521379/
4. Pleuger, Christiane, Fietz, Daniela, Hartmann, Katja, Dorresteijn, Adriaan, Bergmann, Martin. 2016. Expression of katanin p80 in human spermatogenesis. In Fertility and sterility, 106, 1683-1690.e1. doi:10.1016/j.fertnstert.2016.08.043. https://pubmed.ncbi.nlm.nih.gov/27717557/
5. Kaya, Yesim, Korulu, Sirin, Tunoglu, Ezgi Nurdan Yenilmez, Yildiz, Aysegul. 2023. A potential posttranscriptional regulator for p60-katanin: miR-124-3p. In Cytoskeleton (Hoboken, N.J.), 80, 437-447. doi:10.1002/cm.21769. https://pubmed.ncbi.nlm.nih.gov/37439368/
6. Yigit, Gökhan, Wieczorek, Dagmar, Bögershausen, Nina, Nürnberg, Peter, Wollnik, Bernd. 2015. A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation. In American journal of medical genetics. Part A, 170, 728-33. doi:10.1002/ajmg.a.37484. https://pubmed.ncbi.nlm.nih.gov/26640080/