Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis-Reference-Cited by-同舟云学术

Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis

Published:2013-12-13 Issue:2 Volume:261 Page:373-381
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Citterio Andrea,Arnoldi Alessia,Panzeri Elena,D’Angelo Maria Grazia,Filosto Massimiliano,Dilena Robertino,Arrigoni Filippo,Castelli Marianna,Maghini Cristina,Germiniasi Chiara,Menni Francesca,Martinuzzi Andrea,Bresolin Nereo,Bassi Maria Teresa

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-013-7206-6.pdf

Reference22 articles.

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3. Fink JK (2013) Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms. Acta Neuropathol 126(3):307–328. doi: 10.1007/s00401-013-1115-8

4. McDermott C, White K, Bushby K, Shaw P (2000) Hereditary spastic paraparesis: a review of new developments. J Neurol Neurosurg Psychiatry 69(2):150–160. doi: 10.1136/jnnp.69.2.150

5. Boukhris A, Stevanin G, Feki I, Denora P, Elleuch N, Miladi MI, Goizet C, Truchetto J, Belal S, Brice A, Mhiri C (2009) Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity. Clin Genet 75(6):527–536. doi: 10.1111/j.1399-0004.2009.01176.x

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