Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.

Giovanni Stevanin, Hamid Azzedine, Paola Denora, Amir Boukhris, Meriem Tazir, Alexander Lossos, Alberto Luis Rosa, Israela Lerer, Abdelmadjid Hamri, Paulo Alegria, José Loureiro, Masayoshi Tada, Didier Hannequin, Mathieu Anheim, Cyril Goizet, Victoria Gonzalez-Martinez, Isabelle Le Ber, Sylvie Forlani, Kiyoshi Iwabuchi, Vardiela Meiner, Goekhan Uyanik, Anne Kjersti Erichsen, Imed Feki, Florence Pasquier, Soreya Belarbi, Vitor T Cruz, Christel Depienne, Jeremy Truchetto, Guillaume Garrigues, Chantal Tallaksen, Christine Tranchant, Masatoyo Nishizawa, José Vale, Paula Coutinho, Filippo M Santorelli, Chokri Mhiri, Alexis Brice, Alexandra Durr

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DOI: 10.1093/brain/awm293
Published: 2008-03
Container: Brain - A Journal of Neurology
Publisher: Not recorded
Open access: no

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Cite this work

BibTeX

@article{allodium:10.1093/brain/awm293,
  title = {Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.},
  author = {Giovanni Stevanin and Hamid Azzedine and Paola Denora and Amir Boukhris and Meriem Tazir and Alexander Lossos and Alberto Luis Rosa and Israela Lerer and Abdelmadjid Hamri and Paulo Alegria and José Loureiro and Masayoshi Tada and Didier Hannequin and Mathieu Anheim and Cyril Goizet and Victoria Gonzalez-Martinez and Isabelle Le Ber and Sylvie Forlani and Kiyoshi Iwabuchi and Vardiela Meiner and Goekhan Uyanik and Anne Kjersti Erichsen and Imed Feki and Florence Pasquier and Soreya Belarbi and Vitor T Cruz and Christel Depienne and Jeremy Truchetto and Guillaume Garrigues and Chantal Tallaksen and Christine Tranchant and Masatoyo Nishizawa and José Vale and Paula Coutinho and Filippo M Santorelli and Chokri Mhiri and Alexis Brice and Alexandra Durr},
  year = {2008},
  journal = {Brain - A Journal of Neurology},
  doi = {10.1093/brain/awm293},
  url = {https://doi.org/10.1093/brain/awm293}
}

RIS

TY  - JOUR
TI  - Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.
AU  - Giovanni Stevanin
AU  - Hamid Azzedine
AU  - Paola Denora
AU  - Amir Boukhris
AU  - Meriem Tazir
AU  - Alexander Lossos
AU  - Alberto Luis Rosa
AU  - Israela Lerer
AU  - Abdelmadjid Hamri
AU  - Paulo Alegria
AU  - José Loureiro
AU  - Masayoshi Tada
AU  - Didier Hannequin
AU  - Mathieu Anheim
AU  - Cyril Goizet
AU  - Victoria Gonzalez-Martinez
AU  - Isabelle Le Ber
AU  - Sylvie Forlani
AU  - Kiyoshi Iwabuchi
AU  - Vardiela Meiner
AU  - Goekhan Uyanik
AU  - Anne Kjersti Erichsen
AU  - Imed Feki
AU  - Florence Pasquier
AU  - Soreya Belarbi
AU  - Vitor T Cruz
AU  - Christel Depienne
AU  - Jeremy Truchetto
AU  - Guillaume Garrigues
AU  - Chantal Tallaksen
AU  - Christine Tranchant
AU  - Masatoyo Nishizawa
AU  - José Vale
AU  - Paula Coutinho
AU  - Filippo M Santorelli
AU  - Chokri Mhiri
AU  - Alexis Brice
AU  - Alexandra Durr
PY  - 2008
JO  - Brain - A Journal of Neurology
DO  - 10.1093/brain/awm293
UR  - https://doi.org/10.1093/brain/awm293
ER  -

APA

Stevanin, G., Azzedine, H., Denora, P., Boukhris, A., Tazir, M., Lossos, A., Rosa, A. L., Lerer, I., Hamri, A., Alegria, P., Loureiro, J., Tada, M., Hannequin, D., Anheim, M., Goizet, C., Gonzalez-Martinez, V., Ber, I. L., Forlani, S., Iwabuchi, K., Meiner, V., Uyanik, G., Erichsen, A. K., Feki, I., Pasquier, F., Belarbi, S., Cruz, V. T., Depienne, C., Truchetto, J., Garrigues, G., Tallaksen, C., Tranchant, C., Nishizawa, M., Vale, J., Coutinho, P., Santorelli, F. M., Mhiri, C., Brice, A., & Durr, A. (2008). Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.. Brain - A Journal of Neurology. https://doi.org/10.1093/brain/awm293

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hal · retrieved 2026-09-26T03:39:29.018Z