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Mutations in CKAP2L, the human homolog of the mouse radmis gene, cause filippi syndrome
Muhammad Sajid Hussain, Agatino Battaglia, Sandra Szczepanski, Emrah Kaygusuz, Mohammad Reza Toliat, Shin Ichi Sakakibara, Janine Altmüller, Holger Thiele, Gudrun Nürnberg, Shahida Moosa, Gökhan Yigit, Filippo Beleggia, Sigrid Tinschert, Jill Clayton-Smith, Pradeep Vasudevan, Jill E. Urquhart, Dian Donnai, Alan Fryer, Ferda Percin, Francesco Brancati
*Corresponding author for this work
- University of Cologne
- IRCCS Fondazione Stella Maris - Calambrone (Pisa)
- Laboratory for Molecular Neurobiology
- Waseda University
- University of Innsbruck
- Institute for Clinical Genetics
- Universitätsklinikum Carl Gustav Carus
- Manchester Centre for Genomic Medicine
- University of Manchester
- Department of Health Sciences
- University of Liverpool
- Alder Hey Children's Hospital
- Department of Medical Genetics
- Gazi University
- Department of Medical
- Gabriele D'Annunzio University of Chieti-Pescara
- Medical Genetics Unit
- I.N.F.N. Sezione di Rome 'Tor Vergata,'
- Yorkshire Regional Genetics Service
- Chapel Allerton Hospital
- Genetics Department
- Wroclaw Medical University
11
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(Scopus)