The startle disease mutation Q266H, in the second transmembrane domain of the human glycine receptor, impairs channel gating (Q40976356)
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scientific article published on February 1999
- The Startle Disease Mutation Q266H, in the Second Transmembrane Domain of the Human Glycine Receptor, Impairs Channel Gating
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The startle disease mutation Q266H, in the second transmembrane domain of the human glycine receptor, impairs channel gating |
scientific article published on February 1999 |
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The startle disease mutation Q266H, in the second transmembrane domain of the human glycine receptor, impairs channel gating (English)
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The Startle Disease Mutation Q266H, in the Second Transmembrane Domain of the Human Glycine Receptor, Impairs Channel Gating (English)
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Moorhouse AJ
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Jacques P
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Barry PH
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Schofield PR
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1 February 1999
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55
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2
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386-395
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