Pediatric Neurology Briefs (Oct 2001)

Glut-1 Deficiency Syndrome and Familial Epilepsy

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-15-10-2
Journal volume & issue
Vol. 15, no. 10
pp. 74 – 75

Abstract

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A family with autosomal dominant Glut-1 deficiency syndrome (DS) affecting 5 members over 3 generations is reported from the University of Goettingen, Germany; and Columbia University, New York.

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