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Hereditary spastic paraplegia 73
- ... SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum. Neurology. 2009 Oct 6;73(14):1111-9. doi: 10.1212/WNL.0b013e3181bacf59. ...
- ... PubMed Freeman C, Seaman MN, Reid E. The hereditary spastic paraplegia protein strumpellin: characterisation in neurons and of the effect of disease mutations on WASH complex assembly and function. Biochim Biophys Acta. 2013 Jan;1832(1):160-73. doi: 10.1016/j.bbadis.2012.10.011. ...
- ... PubMed Freeman C, Seaman MN, Reid E. The hereditary spastic paraplegia protein strumpellin: characterisation in neurons and of the effect of disease mutations on WASH complex assembly and function. Biochim Biophys Acta. 2013 Jan;1832(1):160-73. doi: 10.1016/j.bbadis.2012.10.011. ...
- ... 4a cause hereditary dystonia. Ann Neurol. 2013 Apr;73(4):546-53. doi: ... complicated hereditary spastic paraplegia. Mov Disord. 2015 May;30(6):854-8. ...
- ... TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia. Mov Disord. 2015 May;30(6):854-8. ...