Publication : Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome.

First Author  Riazuddin S Year  2011
Journal  BMC Med Genet Volume  12
Pages  21 PubMed ID  21306635

1 Bio Entities

Id Name Short Name Type
IPR028232 Fibroblast growth factor 3 FGF3 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)