Netrin-G2 dysfunction causes a Rett-like phenotype with areflexia.

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作者： Gali,Heimer ^[1] ; Geeske M,van Woerden ^[2] ; Ortal,Barel ^[3] ; Dina,Marek-Yagel ^[4] ; Nitzan,Kol ^[5] ; Johannes B,Munting ^[6] ; Minoeshka,Borghei ^[7] ; Osama M,Atawneh ^[8] ; Andreea,Nissenkorn ^[6] ; Gideon,Rechavi ^[7] ; Yair,Anikster ^[4] ; Ype,Elgersma ^[4] ; Steven A,Kushner ^[9] ; Bruria,Ben Zeev ^[1]

作者单位： Pediatric Neurology Unit, Edmond and Lily Safra Children's Hospital, Chaim Sheba Medical Center, Ramat Gan, Israel. ^[1] The Pinchas Borenstein Talpiot Medical Leadership Program, The Chaim Sheba Medical Center, Ramat Gan, Israel. ^[2] The Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel. ^[3] Department of Neuroscience, Erasmus University Medical Center, Rotterdam, The Netherlands. ^[4] ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus University Medical Center, Rotterdam, The Netherlands. ^[5] The Genomic Unit, Sheba Cancer Research Center, Sheba Medical Center, Tel-Hashomer, Israel. ^[6] Wohl Institute for Translational Medicine, Sheba Medical Center, Ramat Gan, Israel. ^[7] Metabolic Disease Unit, Edmond and Lily Safra Children's Hospital, The Chaim Sheba Medical Center, Ramat Gan, Israel. ^[8] Pediatric Department, PRCS Hospital, Hebron, Israel. ^[9] Department of Psychiatry, Erasmus University Medical Center, Rotterdam, The Netherlands. ^[10]

关键词 NTNG2 RTT-like Rett areflexia developmental delay netrin-G