Talk:Multisystem proteinopathy
 | This article is rated Start-class on Wikipedia's content assessment scale. It is of interest to the following WikiProjects: | ||||||||||
| |||||||||||
 | Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Multisystem proteinopathy.
|
 | The contents of the Multisystem proteinopathy page were merged into Hereditary inclusion body myopathy. For the contribution history and old versions of the merged article please see its history. |
Wiki Education Foundation-supported course assignment
This article is or was the subject of a Wiki Education Foundation-supported course assignment. Further details are available on the course page. Student editor(s): Skd17.
Above undated message substituted from Template:Dashboard.wikiedu.org assignment by PrimeBOT (talk) 01:16, 18 January 2022 (UTC)
note
At the moment, the provided information seems accurate and interesting but could be expanded significantly, although some of the sources are not easily accessible. In addition to explaining some of the more basic causes and who is at risk for this degenerative disorder, I would like to explore the known effects of mutations identified in the VCP gene. A lot of the citation for this wikipedia page look to be very strong, yet the article has fairly limited information. Lastly, their are a couple of genes in this article linked to other sources, yet are not associated with a wikipedia page. As they are marked in red it seems like they may have been at some point, but I am not sure. 50.202.217.173 (talk) 20:22, 16 September 2016 (UTC) Skd17 (talk) 20:26, 16 September 2016 (UTC)