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Novel RAB39B Mutation Causes Parkinsonism in Males with Developmental Disorder.
Dayan, Roy; Shkedi Rafid, Shiri; Baker Erdman, Halen; Weill, Caroline; Shag, Avraham; Meiner, Vardiella; Arkadir, David.
Affiliation
  • Dayan R; Department of Neurology, Hadassah Medical Center and the Faculty of Medicine, the Hebrew University, Jerusalem, Israel.
  • Shkedi Rafid S; Department of Genetics, Hadassah Medical Center and the Faculty of Medicine, The Hebrew University, Jerusalem, Israel.
  • Baker Erdman H; The Edmond and Lily Safra Center for Brain Sciences, The Hebrew University, Jerusalem, Israel.
  • Weill C; Department of Neurology, Hadassah Medical Center and the Faculty of Medicine, the Hebrew University, Jerusalem, Israel.
  • Shag A; Department of Genetics, Hadassah Medical Center and the Faculty of Medicine, The Hebrew University, Jerusalem, Israel.
  • Meiner V; Department of Genetics, Hadassah Medical Center and the Faculty of Medicine, The Hebrew University, Jerusalem, Israel.
  • Arkadir D; Department of Neurology, Hadassah Medical Center and the Faculty of Medicine, the Hebrew University, Jerusalem, Israel.
Mov Disord Clin Pract ; 11(3): 306-308, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38293822
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Parkinsonian Disorders Type of study: Etiology_studies Limits: Child / Humans / Male Language: En Journal: Mov Disord Clin Pract Year: 2024 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Parkinsonian Disorders Type of study: Etiology_studies Limits: Child / Humans / Male Language: En Journal: Mov Disord Clin Pract Year: 2024 Document type: Article Affiliation country: Country of publication: