Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2

Dürr, A.; Davoine, C.-S.; Paternotte, C.; Von Fellenberg, J.; Cogilnicean, S.; Coutinho, P.; Lamy, C.; Bourgeois, S.; Prud'Homme, J.-F.; Penet, C.; Mas, J.-L.; Burgunder, J.-M.; Hazan, J.; Weissenbach, J.; Brice, A.; Fontaine, B. (1996). Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2. Brain, 119(5), pp. 1487-1496. Oxford University Press 10.1093/brain/119.5.1487

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Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Head Organs and Neurology (DKNS) > Clinic of Neurology

UniBE Contributor:

Burgunder, Jean-Marc

Subjects:

600 Technology > 610 Medicine & health

ISSN:

0006-8950

Publisher:

Oxford University Press

Language:

English

Submitter:

Markus Müller

Date Deposited:

02 Oct 2018 16:15

Last Modified:

22 Oct 2019 22:17

Publisher DOI:

10.1093/brain/119.5.1487

BORIS DOI:

10.7892/boris.115584

URI:

https://boris.unibe.ch/id/eprint/115584

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