Characterizing the molecular etiology of arthrogryposis multiplex congenita in patients with LGI4 mutations. (2021)

First Author: Booth DG
Attributed to:  The Molecular Basis of Chromosome Periphery Function, Structure and Composition funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/glia.24061

PubMed Identifier: 34288120

Publication URI: http://europepmc.org/abstract/MED/34288120

Type: Journal Article/Review

Volume: 69

Parent Publication: Glia

Issue: 11

ISSN: 0894-1491