Publication : Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.

First Author  Min BJ Year  2011
Journal  Am J Hum Genet Volume  89
Pages  760-6 PubMed ID  22152677
Issue  6

1 Bio Entities

Id Name Short Name Type
IPR026986 Kinesin-like protein KIF22 (Kid) KIF22 Family

To cite PlanMine, please refer to the following publication:

Rozanski, A., Moon, H., Brandl, H., Martín-Durán, J. M., Grohme, M., Hüttner, K., Bartscherer, K., Henry, I., & Rink, J. C.
PlanMine 3.0—improvements to a mineable resource of flatworm biology and biodiversity
Nucleic Acids Research, gky1070. doi:10.1093/nar/gky1070 (2018)