Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum

Zhang, Shu-Shan; Chen, Qin; Chen, Xue-Ping; Wang, Jian-Gang; Burgunder, Jean-Marc; Shang, Hui-Fang (2008). Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum. Movement disorders, 23(6), pp. 917-9. Hoboken, N.J.: Wiley-Blackwell 10.1002/mds.21942

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Item Type:	Journal Article (Further Contribution)
Division/Institute:	04 Faculty of Medicine > Department of Head Organs and Neurology (DKNS) > Clinic of Neurology
UniBE Contributor:	Burgunder, Jean-Marc
ISSN:	0885-3185
ISBN:	18361476
Publisher:	Wiley-Blackwell
Submitter:	Factscience Import
Date Deposited:	04 Oct 2013 15:05
Last Modified:	05 Dec 2022 14:20
Publisher DOI:	10.1002/mds.21942
PubMed ID:	18361476
Web of Science ID:	000255600200027
URI:	https://boris.unibe.ch/id/eprint/28388 (FactScience: 120497)