Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2022-09-01
|
Series: | Frontiers in Molecular Neuroscience |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fnmol.2022.1011856/full |
_version_ | 1798024927645794304 |
---|---|
author | Danique Beijer Stephan L. Züchner |
author_facet | Danique Beijer Stephan L. Züchner |
author_sort | Danique Beijer |
collection | DOAJ |
first_indexed | 2024-04-11T18:10:41Z |
format | Article |
id | doaj.art-38b6633a49ce4f9bb3f755fdbc0455f7 |
institution | Directory Open Access Journal |
issn | 1662-5099 |
language | English |
last_indexed | 2024-04-11T18:10:41Z |
publishDate | 2022-09-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Molecular Neuroscience |
spelling | doaj.art-38b6633a49ce4f9bb3f755fdbc0455f72022-12-22T04:10:07ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992022-09-011510.3389/fnmol.2022.10118561011856Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizuresDanique BeijerStephan L. Züchnerhttps://www.frontiersin.org/articles/10.3389/fnmol.2022.1011856/fullspectrin (α/β)monogenic diseasenext generation sequencing (NGS)neurodevelopmental disordersgenetic data analysisspectrin cytoskeleton |
spellingShingle | Danique Beijer Stephan L. Züchner Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures Frontiers in Molecular Neuroscience spectrin (α/β) monogenic disease next generation sequencing (NGS) neurodevelopmental disorders genetic data analysis spectrin cytoskeleton |
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 | spectrin (α/β) monogenic disease next generation sequencing (NGS) neurodevelopmental disorders genetic data analysis spectrin cytoskeleton |
url | https://www.frontiersin.org/articles/10.3389/fnmol.2022.1011856/full |
work_keys_str_mv | AT daniquebeijer commentarysptbn5encodingthebvspectrinproteinleadstoasyndromeofintellectualdisabilitydevelopmentaldelayandseizures AT stephanlzuchner commentarysptbn5encodingthebvspectrinproteinleadstoasyndromeofintellectualdisabilitydevelopmentaldelayandseizures |