Clinical Variability of GLUT1DS

Investigators from Pavia, Rho, Brescia and Milan, Italy, studied 22 patients diagnosed with GLUT1 deficiency syndrome (GLUT1DS) to document clinical or genetic differences between patients with familial <em>SLC2A1</em> gene mutations (n=11) and those with sporadic mutations (n=11).

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Bibliographic Details
Main Authors: Anastasia Martinez-Esteve Melnikova (Author), Christian M Korff (Author)
Format: Book
Published: Pediatric Neurology Briefs Publishers, 2015-02-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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