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Dive into the research topics of 'Type 1 glucose transporter (Glut1) deficiency: Manifestations of a hereditary neurological syndrome'. Together they form a unique fingerprint.- Sort by
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Juan M. Pascual, B. Lecumberri, D. Wang, R. Yang, K. Engelstad, D. C. De Vivo
Research output: Contribution to journal › Review article › peer-review