Clinical and genetic characterization of SPG11: Hereditary Spastic Paraplegia with thin corpus callosum

Winner B, Winkler J, Uyanik G, Cirak S, Hehr U (2006)

Publication Status: Published

Publication Type: Journal article, other

Publication year: 2006

Journal

Neuromuscular Disorders Elsevier

Publisher: PERGAMON-ELSEVIER SCIENCE LTD

Book Volume: 16

Pages Range: S63-S63

DOI: 10.1055/s-2006-923982

Authors with CRIS profile

Beate Winner Professur für Stammzell-Modelle seltener neuraler Erkrankungen Jürgen Winkler Professur für Molekulare Neurologie

Involved external institutions

Universitätsklinikum Regensburg DE Germany (DE) Universität zu Köln DE Germany (DE) Hanusch-Krankenhaus AT Austria (AT)

How to cite

APA:

Winner, B., Winkler, J., Uyanik, G., Cirak, S., & Hehr, U. (2006). Clinical and genetic characterization of SPG11: Hereditary Spastic Paraplegia with thin corpus callosum. Neuromuscular Disorders, 16, S63-S63. https://doi.org/10.1055/s-2006-923982

MLA:

Winner, Beate, et al. "Clinical and genetic characterization of SPG11: Hereditary Spastic Paraplegia with thin corpus callosum." Neuromuscular Disorders 16 (2006): S63-S63.

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