Parkinson disease: CSMD1 gene mutations can lead to familial Parkinson disease

Patel, Mitesh

dc.contributor.author	Patel, Mitesh
dc.date.accessioned	2019-01-11T11:51:26Z
dc.date.available	2019-01-11T11:51:26Z
dc.date.issued	2017-09-15
dc.identifier.issn	1759-4758	en
dc.identifier.doi	10.1212/NXG.0000000000000177
dc.identifier.uri	http://hdl.handle.net/2436/622048
dc.description	In Brief, comment on original article: Ruiz-Martinez, J. et al. Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson disease. Neurology: Genetics. 2017. Doi: 10.1212/NXG.0000000000000177.	en
dc.format	application/PDF	en
dc.language.iso	en	en
dc.publisher	Springer	en
dc.relation.url	https://www.nature.com/articles/nrneurol.2017.132	en
dc.rights	Attribution-NonCommercial-NoDerivs 3.0 United States	*
dc.rights.uri	http://creativecommons.org/licenses/by-nc-nd/3.0/us/	*
dc.subject	Parkinson's disease	en
dc.subject	familial	en
dc.subject	genetics	en
dc.subject	CSMD1	en
dc.title	Parkinson disease: CSMD1 gene mutations can lead to familial Parkinson disease	en
dc.type	Other	en
dc.identifier.journal	Nature Reviews Neurology	en
pubs.place-of-publication	UK
dc.date.accepted	2017-09-15
rioxxterms.funder	University of Wolverhampton	en
rioxxterms.identifier.project	UOW110119MP	en
rioxxterms.version	AM	en
rioxxterms.licenseref.uri	https://creativecommons.org/licenses/by-nc-nd/4.0/	en
rioxxterms.licenseref.startdate	2019-01-11	en
refterms.dateFCD	2019-01-11T11:51:27Z
refterms.versionFCD	AM
refterms.dateFOA	2019-01-11T11:51:27Z