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Mutations in SPG11 are frequent in autosomal recessive spas..:
Stevanin, Giovanni
;
Azzedine, Hamid
;
Denora, Paola
...
Brain. 131 (2007) 3 - p. 772-784 , 2007
Link:
https://doi.org/10.1093/brain/awm293
RT Journal T1
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_brain_awm293&Exemplar=1&LAN=DE A1 Stevanin, Giovanni A1 Azzedine, Hamid A1 Denora, Paola A1 Boukhris, Amir A1 Tazir, Meriem A1 Lossos, Alexander A1 Rosa, Alberto Luis A1 Lerer, Israela A1 Hamri, Abdelmadjid A1 Alegria, Paulo A1 Loureiro, José A1 Tada, Masayoshi A1 Hannequin, Didier A1 Anheim, Mathieu A1 Goizet, Cyril A1 Gonzalez-Martinez, Victoria A1 Le Ber, Isabelle A1 Forlani, Sylvie A1 Iwabuchi, Kiyoshi A1 Meiner, Vardiela A1 Uyanik, Goekhan A1 Erichsen, Anne Kjersti A1 Feki, Imed A1 Pasquier, Florence A1 Belarbi, Soreya A1 Cruz, Vitor T. A1 Depienne, Christel A1 Truchetto, Jeremy A1 Garrigues, Guillaume A1 Tallaksen, Chantal PB Oxford University Press (OUP) YR 2007 SN 1460-2156 SN 0006-8950 JF Brain VO 131 IS 3 SP 772 OP 784 LK http://dx.doi.org/https://doi.org/10.1093/brain/awm293 DO https://doi.org/10.1093/brain/awm293 SF ELIB - SuUB Bremen
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