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Find link is a tool written by Edward Betts .
searching for GLUT1 deficiency 4 found (21 total)
alternate case: gLUT1 deficiency
Neuroglycopenia
(764 words)
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hypoglycorrhacia]. Hypoglycorrhachia is associated with Glucose transporter type 1 GLUT1 deficiency syndrome (De Vivo disease). Perhaps a much more common example of the
Major facilitator superfamily
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Wang D, Lecumberri B, Yang H, Mao X, Yang R, De Vivo DC (May 2004). "GLUT1 deficiency and other glucose transporter diseases". European Journal of Endocrinology
Microcephaly
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syndrome". Orphanet. Retrieved 2019-08-01. Reference, Genetics Home. "GLUT1 deficiency syndrome". Genetics Home Reference. Retrieved 2019-08-01. "Maternal
List of OMIM disorder codes
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Glucose-galactose malabsorption; 606824; SLC5A1 GLUT1 deficiency syndrome 1; 606777; SLC2A1 GLUT1 deficiency syndrome 2; 612126; SLC2A1 Glutamate formiminotransferase