In der Literatur taucht KIF11 bisher lediglich in englischsprachigen Artikeln auf.
Die drei wichtigsten Literaturquellen, sind unten aufgeführt.

Was bisher bekannt ist:

Ostergaard, P., Simpson, M. A., Mendola, A., Vasudevan, P., Connell, F. C., van Impel, A., … Jeffery, S. (2012). Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy. American journal of human genetics, 90(2), 356–362. doi:10.1016/j.ajhg.2011.12.018

Jones, G. E., Ostergaard, P., Moore, A. T., Connell, F. C., Williams, D., Quarrell, O., … Mansour, S. (2014). Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations. European journal of human genetics : EJHG, 22(7), 881–887. doi:10.1038/ejhg.2013.263

Birtel J, Gliem M, Mangold E, Tebbe L, Spier I, Müller PL, Holz FG, Neuhaus C, Wolfrum U, Bolz HJ, Charbel Issa P (2017) Novel Insights Into the Phenotypical Spectrum of KIF11-Associated Retinopathy, Including a New Form of Retinal Ciliopathy.

1;58(10):3950-3959. doi: 10.1167/iovs.17-21679