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

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