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GLUT1 Deficiency in a Patient Diagnosed as Cerebral Palsy: Is NGS a Valuable Tool to Be Considered in All Cases of CP to Detect Underlying Genetic Disorders?
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| Publicat a: | Mov Disord Clin Pract |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley & Sons, Inc.
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6476600/ https://ncbi.nlm.nih.gov/pubmed/31061833 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.12754 |
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