Recessive hyperekplexia mutations of the glycine receptor α1 subunit affect cell surface integration and stability
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-4159.2009.06372.x/fullpdf
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2. The inhibitory glycine receptor as a model of hereditary channelopathies
3. Identification of the microdeletion breakpoint in a GLRA1null allele of Turkish hyperekplexia patients;Becker;Hum. Mutat.,2006
4. Glycine receptors: recent insights into their structural organization and functional diversity;Betz;J. Neurochem.,2006
5. Statistical coassembly of glycine receptor alpha1 wildtype and the hyperekplexia mutant alpha1(P250T) in HEK 293 cells: impaired channel function is not dominant in the recombinant system;Breitinger;Neurosci. Lett.,2002a
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