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

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Description scientific article published on 13 December 2007
Author/s

author: José L. Loureiro  Vítor T. Cruz  Didier Hannequin  Chokri Mhiri  Mathieu Anheim  Florence Pasquier  Paula Coutinho  Filippo Maria Santorelli  Christine Tranchant  Alexandra Durr  Sylvie Forlani  Giovanni Stevanin  Christel Depienne  Abdelmadjid Hamri  Soraya Belarbi  Amir Boukhris  Israela Lerer  Jérémy Truchetto  Masatoyo Nishizawa  Alexis Brice  Isabelle Le Ber  Alexander Lossos  Chantal M E Tallaksen  Imed Feki  Hamid Azzedine  Paola S Denora  Paulo Alegria  Anne Kjersti Erichsen  Cyril Goizet  Meriem Tazir 

Publication date December 13, 2007
Language English
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