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

Front Mol Neurosci. 2022 Sep 27:15:1017684. doi: 10.3389/fnmol.2022.1017684. eCollection 2022.

Authors

Liedewei Van De Vondel^{1

2}, Jonathan De Winter^{1

2

3}, Jonathan Baets^{1

2

3}

Affiliations

¹ Department of Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Edegem, Belgium.
² Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.
³ Department of Neurology, NeuroMuscular Reference Center, Antwerp University Hospital, Edegem, Belgium.

No abstract available

Keywords: SPTBN5; intellectual disability (ID); rare diseases (RD); spectrin; whole exome sequencing.

Publication types

Comment