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Novel translational phenotypes and biomarkers for creatine transporter deficiency
Creatine transporter deficiency is a metabolic disorder characterized by intellectual disability, autistic-like behaviour and epilepsy. There is currently no cure for creatine transporter deficiency, and reliable biomarkers of translational value for monitoring disease progression and response to th...
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| Publicado no: | Brain Commun |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7472907/ https://ncbi.nlm.nih.gov/pubmed/32954336 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/braincomms/fcaa089 |
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