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ArticleMovement disorders clinical practice2019

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?

Aurélie Méneret et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2019
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Full record →Abstract, authors, funding and every citing paper · PMID 31061833