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searching for GLUT1 deficiency 4 found (21 total)

alternate case: gLUT1 deficiency

Neuroglycopenia (764 words) [view diff] exact match in snippet view article find links to article

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 (5,029 words) [view diff] exact match in snippet view article find links to article
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 (4,199 words) [view diff] exact match in snippet view article find links to article
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 (18,877 words) [view diff] exact match in snippet view article find links to article
Glucose-galactose malabsorption; 606824; SLC5A1 GLUT1 deficiency syndrome 1; 606777; SLC2A1 GLUT1 deficiency syndrome 2; 612126; SLC2A1 Glutamate formiminotransferase