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:

21 Jan 2015 11:08

Publisher DOI:

10.1002/mds.21942

PubMed ID:

18361476

Web of Science ID:

000255600200027

URI:

https://boris.unibe.ch/id/eprint/28388 (FactScience: 120497)

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