Jump to content

Talk:Ryanodine receptor 2

Page contents not supported in other languages.
From Wikipedia, the free encyclopedia

Suggestions for improvement

[edit]

Great recents edits to this article! I'd be interested to read about how different mutations to RYR2 lead to the various clinic conditions, if these have been studied. Also, since we mostly care about RYR2 because it can become dysfunctional, it might be worth mentioning its relevance to clinical medicine in the introductory paragraph. — Preceding unsigned comment added by Laundromatzat (talkcontribs) 23:48, 24 February 2015 (UTC)[reply]