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

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:
spectrin (α/β)
monogenic disease
next generation sequencing (NGS)
neurodevelopmental disorders
genetic data analysis
spectrin cytoskeleton
Online Access:https://www.frontiersin.org/articles/10.3389/fnmol.2022.1011856/full
Description
ISSN:1662-5099

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