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Mouse models of GNAO1-associated movement disorder: Allele- and sex-specific differences in phenotypes
BACKGROUND: Infants and children with dominant de novo mutations in GNAO1 exhibit movement disorders, epilepsy, or both. Children with loss-of-function (LOF) mutations exhibit Epileptiform Encephalopathy 17 (EIEE17). Gain-of-function (GOF) mutations or those with normal function are found in patient...
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| Publicado no: | PLoS One |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6347370/ https://ncbi.nlm.nih.gov/pubmed/30682176 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0211066 |
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