Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia

Francesc Pérez‐Brangulí(Friedrich-Alexander-Universität Erlangen-Nürnberg), Beate Winner(Friedrich-Alexander-Universität Erlangen-Nürnberg)
Human Molecular Genetics
May 2, 2014
Cited by 117


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