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The startle disease mutation Q266H, in the second transmembrane domain of the human glycine receptor, impairs channel gating.
Moorhouse, A J; Jacques, P; Barry, P H; Schofield, P R.
Affiliation
  • Moorhouse AJ; School of Physiology and Pharmacology, University of New South Wales, Sydney, Australia.
Mol Pharmacol ; 55(2): 386-95, 1999 Feb.
Article in En | MEDLINE | ID: mdl-9927632
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Collection: 01-internacional Database: MEDLINE Main subject: Reflex, Startle / Ion Channel Gating / Receptors, Glycine Limits: Humans Language: En Journal: Mol Pharmacol Year: 1999 Document type: Article Affiliation country: Australia Country of publication: Estados Unidos
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Collection: 01-internacional Database: MEDLINE Main subject: Reflex, Startle / Ion Channel Gating / Receptors, Glycine Limits: Humans Language: En Journal: Mol Pharmacol Year: 1999 Document type: Article Affiliation country: Australia Country of publication: Estados Unidos