A 23 years follow-up study identifies GLUT1 deficiency...

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European Journal of Medical Genetics 2016 / 10

A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia

Diomedi, Marina, Gan-Or, Ziv, Placidi, Fabio, Dion, Patrick A., Szuto, Anna, Bengala, Mario, Rouleau, Guy A., Gigli, Gian Luigi
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Language:
english
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2016.10.003
Date:
October, 2016
File:
PDF, 1.00 MB
english, 2016
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