Structural Insights into Genetic Variants of Na+/Glucose Cotransporter SGLT1 Causing Glucose–Galactose Malabsorption: vSGLT as a Model Structure
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Biochemistry,General Medicine,Biophysics
Link
http://link.springer.com/content/pdf/10.1007/s12013-012-9352-3.pdf
Reference34 articles.
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2. Wright, E. M., & Turk, E. (2004). The sodium/glucose cotransport family SLC5. Pflügers Archiv, 447, 510–518.
3. Turk, E., & Wright, E. M. (1997). Membrane topology motifs in the SGLT cotransporter family. Journal of Membrane Biology, 159, 1–20.
4. Banerjee, S. K., McGaffin, K. R., Pastor-Soler, N. M., & Ahmad, F. (2009). SGLT1 is a novel cardiac glucose transporter that is perturbed in disease states. Cardiovascular Research, 84, 111–118.
5. Martin, M. G., Turk, E., Lostao, M. P., Kerner, C., & Wright, E. M. (1996). Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose–galactose malabsorption. Nature Genetics, 12, 216–220.
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