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

Journal article

Peer reviewed

Frontiers in molecular neuroscience, Vol.15, p.1011856

2022-09-02

PMID: 36117916

Abstract

Molecular Neuroscience

url

https://doi.org/10.3389/fnmol.2022.1011856View

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Title: Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures
Creators: Danique Beijer - University of Miami
Stephan L. Züchner - Dr. John T. Macdonald Foundation
Publication Details: Frontiers in molecular neuroscience, Vol.15, p.1011856
Publisher: Frontiers Media S.A
Academic Unit: Leadership Department; Miller School of Medicine; John P. Hussman Institute for Human Genomics
Language: English
Resource Type: Journal article
PMID: 36117916
Record Identifier: 991032860799402976