Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy
Titel:
Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy
Auteur:
Ostergaard, Pia Simpson, Michael A. Mendola, Antonella Vasudevan, Pradeep Connell, Fiona C. van Impel, Andreas Moore, Anthony T. Loeys, Bart L. Ghalamkarpour, Arash Onoufriadis, Alexandros Martinez-Corral, Ines Devery, Sophie Leroy, Jules G. van Laer, Lut Singer, Amihood Bialer, Martin G. McEntagart, Meriel Quarrell, Oliver Brice, Glen Trembath, Richard C. Schulte-Merker, Stefan Makinen, Taija Vikkula, Miikka Mortimer, Peter S. Mansour, Sahar Jeffery, Steve