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Glucose transporter‐1 deficiency syndrome with extreme ph... | ResearchHub
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Glucose transporter‐1 deficiency syndrome with extreme phenotypic variability in a five‐generation family carrying a novel SLC2A1 variant
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Authors
Alessia Giugno
9 more
Alessia Giugno
•
Elena Falcone
7 more
•
Antonio Gambardella
Published
May 27, 2024
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Journal
European Journal of Neurology
Topics
Biology
Neuroscience
Medicine
Biochemistry
Physiology
Show all topics
DOI
10.1111/ene.16325
License
CC-BY
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Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
European Journal of Neurology
Topics
Biology
Neuroscience
Medicine
Biochemistry
Physiology
Show all topics
DOI
10.1111/ene.16325
License
CC-BY
Other Formats
PDF
