Glycine receptor, alpha 1: Difference between revisions
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==References== |
==References== |
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*{{cite web | url = http://www.iuphar-db.org/IC/ObjectDisplayForward?familyId=9&objectId=202| title = IUPHAR-DB: α1 subunit > | accessdate = | author = | authorlink = | coauthors = | date = | format = | work = IUPHAR Database of Receptors and Ion Channels | publisher = International Union of Basic and Clinical Pharmacology | pages = | language = | archiveurl = | archivedate = | quote = }} |
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==Further reading== |
==Further reading== |
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Revision as of 15:02, 18 August 2009
Template:PBB Glycine receptor, alpha 1 (startle disease/hyperekplexia, stiff man syndrome), also known as GLRA1, is a human gene.
See also
References
- "IUPHAR-DB: α1 subunit >". IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology.
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Further reading
 | This membrane protein–related article is a stub. You can help Wikipedia by expanding it. |
This article incorporates text from the United States National Library of Medicine, which is in the public domain.