Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners

By Sanderson Christopher M.   Connell James W.   Bright Nicholas A.   Duley Simon   Thompson Amanda   Luzio J. Paul   Reid Evan  

Human Molecular Genetics, Vol. 15, Iss. 2, 2006-01 ,pp. : 307-318

Oxford University Press

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Functional conservation of human Spastin in a Drosophila model of autosomal dominant-hereditary spastic paraplegia

By Du Fang   Ozdowski Emily F.   Kotowski Ingrid K.   Marchuk Douglas A.   Sherwood Nina Tang  

Human Molecular Genetics, Vol. 19, Iss. 10, 2010-05 ,pp. : 1883-1896

Oxford University Press

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The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B

By Reid Evan  

Human Molecular Genetics, Vol. 14, Iss. 1, 2005-01 ,pp. : 19-38

Oxford University Press

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Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

By Fonknechten Nùria  

Human Molecular Genetics, Vol. 9, Iss. 4, 2000-03 ,pp. : 637-644

Oxford University Press

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Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

By Fonknechten Nùria   Mavel Delphine   Byrne Paula   Davoine Claire-Sophie   Cruaud Corinne   Bönsch Dominikus   Samson Delphine   Coutinho Paula   Hutchinson Michael   McMonagle Paul   Burgunder Jean-Marc   Tartaglione Antonio   Heinzlef Olivier   Feki Imed   Deufel Thomas   Parfrey Nollaig   Brice Alexis   Fontaine Bertrand   Prud'homme Jean-François   Weissenbach Jean   Dürr Alexandra   Hazan Jamilé  

Human Molecular Genetics, Vol. 14, Iss. 3, 2005-02 ,pp. : 461-461

Oxford University Press

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