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GRIN2A: An aptly named gene for speech dysfunction
OBJECTIVE: To delineate the specific speech deficits in individuals with epilepsy-aphasia syndromes associated with mutations in the glutamate receptor subunit gene GRIN2A. METHODS: We analyzed the speech phenotype associated with GRIN2A mutations in 11 individuals, aged 16 to 64 years, from 3 famil...
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| Publicado no: | Neurology |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Lippincott Williams & Wilkins
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4335991/ https://ncbi.nlm.nih.gov/pubmed/25596506 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000001228 |
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