Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
about
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.Molecular Dynamics Simulations of the Human Glucose Transporter GLUT1Predicting the three-dimensional structure of the human facilitative glucose transporter glut1 by a novel evolutionary homology strategy: insights on the molecular mechanism of substrate migration, and binding sites for glucose and inhibitory molecuStructural signatures and membrane helix 4 in GLUT1: inferences from human blood-brain glucose transport mutantsFunctional consequences of an in vivo mutation in exon 10 of the human GLUT1 gene.
P2860
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
description
2001 nî lūn-bûn
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2001 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2001年の論文
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2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
@ast
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
@en
type
label
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
@ast
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
@en
prefLabel
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
@ast
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
@en
P2093
P2860
P1433
P1476
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
@en
P2093
P2860
P304
P356
10.1016/S0014-5793(01)02463-2
P407
P577
2001-06-01T00:00:00Z