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Novel RAB39B Mutation Causes Parkinsonism in Males with Developmental Disorder.

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Title: Novel RAB39B Mutation Causes Parkinsonism in Males with Developmental Disorder.
Authors: 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.
Source: Movement disorders clinical practice [Mov Disord Clin Pract] 2024 Mar; Vol. 11 (3), pp. 306-308. Date of Electronic Publication: 2024 Jan 31.
Publication Type: Letter
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 101630279 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2330-1619 (Electronic) Linking ISSN: 23301619 NLM ISO Abbreviation: Mov Disord Clin Pract Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Novel RAB39B Mutation Causes Parkinsonism in Males with Developmental Disorder.
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  Data: <searchLink fieldCode="AU" term="%22Dayan+R%22">Dayan R</searchLink>; Department of Neurology, Hadassah Medical Center and the Faculty of Medicine, the Hebrew University, Jerusalem, Israel.<br /><searchLink fieldCode="AU" term="%22Shkedi+Rafid+S%22">Shkedi Rafid S</searchLink>; Department of Genetics, Hadassah Medical Center and the Faculty of Medicine, The Hebrew University, Jerusalem, Israel.<br /><searchLink fieldCode="AU" term="%22Baker+Erdman+H%22">Baker Erdman H</searchLink>; The Edmond and Lily Safra Center for Brain Sciences, The Hebrew University, Jerusalem, Israel.<br /><searchLink fieldCode="AU" term="%22Weill+C%22">Weill C</searchLink>; Department of Neurology, Hadassah Medical Center and the Faculty of Medicine, the Hebrew University, Jerusalem, Israel.<br /><searchLink fieldCode="AU" term="%22Shag+A%22">Shag A</searchLink>; Department of Genetics, Hadassah Medical Center and the Faculty of Medicine, The Hebrew University, Jerusalem, Israel.<br /><searchLink fieldCode="AU" term="%22Meiner+V%22">Meiner V</searchLink>; Department of Genetics, Hadassah Medical Center and the Faculty of Medicine, The Hebrew University, Jerusalem, Israel.<br /><searchLink fieldCode="AU" term="%22Arkadir+D%22">Arkadir D</searchLink>; Department of Neurology, Hadassah Medical Center and the Faculty of Medicine, the Hebrew University, Jerusalem, Israel.
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  Data: <searchLink fieldCode="JN" term="%22101630279%22">Movement disorders clinical practice</searchLink> [Mov Disord Clin Pract] 2024 Mar; Vol. 11 (3), pp. 306-308. <i>Date of Electronic Publication: </i>2024 Jan 31.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley%22">Wiley </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101630279 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2330-1619 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2223301619%22">23301619 </searchLink><i>NLM ISO Abbreviation: </i>Mov Disord Clin Pract <i>Subsets: </i>MEDLINE
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        Value: 10.1002/mdc3.13953
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              Text: 2024 Mar
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