Crossmark

Mouse models characterize GNAO1 encephalopathy as a neurodevelopmental disorder leading to motor anomalies: from a severe G203R to a milder C215Y mutation

Crossref DOI link: https://doi.org/10.1186/s40478-022-01312-z

Published Online: 2022-01-28

Published Print: 2022-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Silachev, Denis

Koval, Alexey

Savitsky, Mikhail

Padmasola, Guru

Quairiaux, Charles

Thorel, Fabrizio

Katanaev, Vladimir L. http://orcid.org/0000-0002-7909-5617
Funding

Funding for this research was provided by:

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (31003A_175658)

Russian Science Foundation (21-15-00138)
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Text and Data Mining valid from 2022-01-28

Version of Record valid from 2022-01-28
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Article History

Received: 17 November 2021

Accepted: 8 January 2022

First Online: 28 January 2022

Declarations

:

: The authors declare that they have no Competing interests.

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