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: Liedewei Van De Vondel, Jonathan De Winter, Jonathan Baets
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-09-01
Series:Frontiers in Molecular Neuroscience
Subjects:
SPTBN5
whole exome sequencing
spectrin
intellectual disability (ID)
rare diseases (RD)
Online Access:https://www.frontiersin.org/articles/10.3389/fnmol.2022.1017684/full

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