Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures

Bibliographic Details
Main Authors: Danique Beijer, Stephan L. Züchner
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
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author Danique Beijer
Stephan L. Züchner
author_facet Danique Beijer
Stephan L. Züchner
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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
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