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Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia
Schule, R, Schlipf, N, Synofzik, M, Klebe, S, Klimpe, S, Hehr, U, Winner, B
, Lindig, T, Dotzer, A, Riess, O, Winkler, J, Schols, L and Bauer, P
(2009)
Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia.
Journal of Neurology, Neurosurgery & Psychiatry 80 (12), pp. 1402-1404.
Date of publication of this fulltext: 19 Dec 2024 11:58
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| Item type | Article | ||||
| Journal or Publication Title | Journal of Neurology, Neurosurgery & Psychiatry | ||||
| Publisher: | BMJ PUBLISHING GROUP | ||||
|---|---|---|---|---|---|
| Place of Publication: | LONDON | ||||
| Volume: | 80 | ||||
| Number of Issue or Book Chapter: | 12 | ||||
| Page Range: | pp. 1402-1404 | ||||
| Date | 2009 | ||||
| Institutions | Medicine > Lehrstuhl für Humangenetik Medicine > Lehrstuhl für Neurologie | ||||
| Identification Number |
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| Keywords | MOTOR-NEURON DEGENERATION; THIN CORPUS-CALLOSUM; PREDICTION; SEQUENCE; GENE; IDENTIFICATION; HETEROGENEITY; FAMILIES; CYP7B1; | ||||
| Dewey Decimal Classification | 600 Technology > 610 Medical sciences Medicine | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 66726 |
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