SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome

Ohad Wormser(Ben-Gurion University of the Negev), Libe Gradstein(Soroka Medical Center), Yuval Yogev(Ben-Gurion University of the Negev), Yonatan Perez(Ben-Gurion University of the Negev), Rotem Kadir(Ben-Gurion University of the Negev), Inna Goliand(Ben-Gurion University of the Negev), Yair Sadka(Ben-Gurion University of the Negev), Saad El Riati(Clalit Health Services), Hagit Flusser(Ben-Gurion University of the Negev), Dikla Nachmias(Ben-Gurion University of the Negev), Ruth Birk(Ariel University), Muhamad Iraqi(Ben-Gurion University of the Negev), Einat Kadar(Ben-Gurion University of the Negev), Roni Gat(Ben-Gurion University of the Negev), Max Drabkin(Ben-Gurion University of the Negev), Daniel Halpérin(Ben-Gurion University of the Negev), Amir Horev(Ben-Gurion University of the Negev), Sara Sivan(Ben-Gurion University of the Negev), Uri Abdu(Ben-Gurion University of the Negev), Natalie Elia(Ben-Gurion University of the Negev), Ohad S. Birk(Ben-Gurion University of the Negev)
European Journal of Human Genetics
February 5, 2019
Cited by 48Open Access
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