Novel RAB39B Mutation Causes Parkinsonism in Males with Developmental Disorder.
Saved in:
| 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 |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 2330-1619 |
|---|---|
| DOI: | 10.1002/mdc3.13953 |
