Characterizing the molecular etiology of arthrogryposis multiplex congenita in patients with LGI4 mutations-Reference-Cited by-同舟云学术

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Characterizing the molecular etiology of arthrogryposis multiplex congenita in patients with LGI4 mutations

Published:2021-07-21 Issue:11 Volume:69 Page:2605-2617
ISSN:0894-1491
Container-title:Glia
language:en
Short-container-title:Glia

Author:

Booth Daniel G.¹^ORCID,Kozar Nina¹,Bradley Stephen¹,Meijer Dies¹^ORCID

Affiliation:

1. Centre for Discovery Brain Sciences and MS Society Edinburgh Centre for MS Research University of Edinburgh Edinburgh United Kingdom

Funder

Biotechnology and Biological Sciences Research Council

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/glia.24061

Reference57 articles.

1. Predicting Functional Effect of Human Missense Mutations Using PolyPhen‐2

2. ADAM function in embryogenesis

3. The claw paw mutation reveals a role for Lgi4 in peripheral nerve development

4. Role of integrins in periphral nerves and hereditary neuropathies

5. mScarlet: a bright monomeric red fluorescent protein for cellular imaging

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