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

Bibliographische Detailangaben

Veröffentlicht in:	Brain (London, England : 1878) England : 1878), 2008, Vol.131, p.772-784
Hauptverfasser:	STEVANIN, Giovanni, AZZEDINE, Hamid, LOUREIRO, José, TADA, Masayoshi, HANNEQUIN, Didier, ANHEIM, Mathieu, GOIZET, Cyril, GONZALEZ-MARTINEZ, Victoria, LE BER, Isabelle, FORLANI, Sylvie, IWABUCHI, Kiyoshi, MEINER, Vardiela, DENORA, Paola, UYANIK, Goekhan, KJERSTI ERICHSEN, Anne, FEKI, Imed, PASQUIER, Florence, BELARBI, Soreya, CRUZ, Vitor T, DEPIENNE, Christel, TRUCHETTO, Jeremy, GARRIGUES, Guillaume, TALLAKSEN, Chantal, BOUKHRIS, Amir, TRANCHANT, Christine, NISHIZAWA, Masatoyo, VALE, José, COUTINHO, Paula, SANTORELLI, Filippo M, MHIRI, Chokri, BRICE, Alexis, DURR, Alexandra, TAZIR, Meriem, LOSSOS, Alexander, ROSA, Alberto Luis, LERER, Israela, HAMRI, Abdelmadjid, ALEGRIA, Paulo
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Medical sciences Neurology
Online-Zugang:	Volltext
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