Upstream SLC2A1 translation initiation causes GLUT1 deficiency syndrome.
Willemsen, Michèl A
Upstream SLC2A1 translation initiation causes GLUT1 deficiency syndrome. [electronic resource] - European journal of human genetics : EJHG 06 2017 - 771-774 p. digital
Publication Type: Journal Article
1476-5438
10.1038/ejhg.2017.45 doi
5' Untranslated Regions
Adolescent
Carbohydrate Metabolism, Inborn Errors--diagnosis
Cells, Cultured
Codon, Initiator--genetics
Female
Glucose Transporter Type 1--genetics
Humans
Monosaccharide Transport Proteins--deficiency
Mutation
Peptide Chain Initiation, Translational
Upstream SLC2A1 translation initiation causes GLUT1 deficiency syndrome. [electronic resource] - European journal of human genetics : EJHG 06 2017 - 771-774 p. digital
Publication Type: Journal Article
1476-5438
10.1038/ejhg.2017.45 doi
5' Untranslated Regions
Adolescent
Carbohydrate Metabolism, Inborn Errors--diagnosis
Cells, Cultured
Codon, Initiator--genetics
Female
Glucose Transporter Type 1--genetics
Humans
Monosaccharide Transport Proteins--deficiency
Mutation
Peptide Chain Initiation, Translational