Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures
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| Format: | Article |
| Language: | English |
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Frontiers Media S.A.
2022-09-01
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| Series: | Frontiers in Molecular Neuroscience |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fnmol.2022.1017684/full |
| _version_ | 1811208613787598848 |
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| author | Liedewei Van De Vondel Liedewei Van De Vondel Jonathan De Winter Jonathan De Winter Jonathan De Winter Jonathan Baets Jonathan Baets Jonathan Baets |
| author_facet | Liedewei Van De Vondel Liedewei Van De Vondel Jonathan De Winter Jonathan De Winter Jonathan De Winter Jonathan Baets Jonathan Baets Jonathan Baets |
| author_sort | Liedewei Van De Vondel |
| collection | DOAJ |
| first_indexed | 2024-04-12T04:24:31Z |
| format | Article |
| id | doaj.art-742f90b6d61047bba2f25aeb37b1d21e |
| institution | Directory Open Access Journal |
| issn | 1662-5099 |
| language | English |
| last_indexed | 2024-04-12T04:24:31Z |
| publishDate | 2022-09-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Molecular Neuroscience |
| spelling | doaj.art-742f90b6d61047bba2f25aeb37b1d21e2022-12-22T03:48:08ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992022-09-011510.3389/fnmol.2022.10176841017684Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizuresLiedewei Van De Vondel0Liedewei Van De Vondel1Jonathan De Winter2Jonathan De Winter3Jonathan De Winter4Jonathan Baets5Jonathan Baets6Jonathan Baets7Department of Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Edegem, BelgiumLaboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, BelgiumDepartment of Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Edegem, BelgiumLaboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, BelgiumDepartment of Neurology, NeuroMuscular Reference Center, Antwerp University Hospital, Edegem, BelgiumDepartment of Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Edegem, BelgiumLaboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, BelgiumDepartment of Neurology, NeuroMuscular Reference Center, Antwerp University Hospital, Edegem, Belgiumhttps://www.frontiersin.org/articles/10.3389/fnmol.2022.1017684/fullSPTBN5whole exome sequencingspectrinintellectual disability (ID)rare diseases (RD) |
| spellingShingle | Liedewei Van De Vondel Liedewei Van De Vondel Jonathan De Winter Jonathan De Winter Jonathan De Winter Jonathan Baets Jonathan Baets Jonathan Baets Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures Frontiers in Molecular Neuroscience SPTBN5 whole exome sequencing spectrin intellectual disability (ID) rare diseases (RD) |
| title | Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures |
| title_full | Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures |
| title_fullStr | Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures |
| title_full_unstemmed | Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures |
| title_short | Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures |
| title_sort | commentary sptbn5 encoding the βv spectrin protein leads to a syndrome of intellectual disability developmental delay and seizures |
| topic | SPTBN5 whole exome sequencing spectrin intellectual disability (ID) rare diseases (RD) |
| url | https://www.frontiersin.org/articles/10.3389/fnmol.2022.1017684/full |
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