Home > A. Molecular pathology > KIF11
KIF11
10q24.1 HGNC:6388 MIM.148760
Monday 6 February 2012
kinesin family member 11; "kinesin-like 1", KNSL1; Eg5, HKSP, TRIP5
Pathology
Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy. (22284827)
See also
KIFs
References
Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy. Ostergaard P, Simpson MA, Mendola A, Vasudevan P, Connell FC, van Impel A, Moore AT, Loeys BL, Ghalamkarpour A, Onoufriadis A, Martinez-Corral I, Devery S, Leroy JG, van Laer L, Singer A, Bialer MG, McEntagart M, Quarrell O, Brice G, Trembath RC, Schulte-Merker S, Makinen T, Vikkula M, Mortimer PS, Mansour S, Jeffery S. Am J Hum Genet. 2012 Jan 24. PMID: 22284827