Chloride channels: An emerging molecular picture

Author:

Jentsch Thomas J.,Günther Willy

Publisher

Wiley

Subject

General Biochemistry, Genetics and Molecular Biology

Reference80 articles.

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4. Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurological disorder, hyperekplexia;Shiang;Nature Genet.,1993

5. A GLRA1 null mutation in recessive hyperekplexia challenges the functional role of glycine receptors;Brune;Am. J. Hum. Genet.,1996

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