Publication : Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations.

First Author  Unger S Year  2008
Journal  Nat Genet Volume  40
Pages  287-9 PubMed ID  18297069
Issue  3

1 Bio Entities

Id Name Short Name Type
IPR028759 Cyclin-related protein FAM58 Cyclin-rel_FAM58 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)