Netrin‐G2 dysfunction causes a Rett‐like phenotype with areflexia

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

作者单位： The Genomic Unit, Sheba Cancer Research CenterSheba Medical CenterTel‐Hashomer,Israel ^[1] The Sackler School of MedicineTel Aviv UniversityTel Aviv,Israel ^[2] Pediatric Neurology Unit, Edmond and Lily Safra Children's HospitalChaim Sheba Medical CenterRamat ^[3] Department of NeuroscienceErasmus University Medical CenterRotterdam,The Netherlands ^[4] Metabolic Disease Unit, Edmond and Lily Safra Children's HospitalThe Chaim Sheba Medical ^[5] Pediatric DepartmentPRCS HospitalHebron,Israel ^[6] ENCORE Expertise Center for Neurodevelopmental DisordersErasmus University Medical CenterRotterdam ^[7]

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

发布时间 2020-06-03

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