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| Title : Genetic and phenotypic characterization of complex hereditary spastic paraplegia - Kara_2016_Brain_139_1904 |
| Author(s) : Kara E , Tucci A , Manzoni C , Lynch DS , Elpidorou M , Bettencourt C , Chelban V , Manole A , Hamed SA , Haridy NA , Federoff M , Preza E , Hughes D , Pittman A , Jaunmuktane Z , Brandner S , Xiromerisiou G , Wiethoff S , Schottlaender L , Proukakis C , Morris H , Warner T , Bhatia KP , Korlipara LV , Singleton AB , Hardy J , Wood NW , Lewis PA , Houlden H |
| Ref : Brain , 139 :1904 , 2016 |
| Abstract : Kara_2016_Brain_139_1904 |
| ESTHER : Kara_2016_Brain_139_1904 |
| PubMedSearch : Kara_2016_Brain_139_1904 |
| PubMedID: 27217339 |
| Title : Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia - Simpson_2003_Am.J.Hum.Genet_73_1147 |
| Author(s) : Simpson MA , Cross H , Proukakis C , Pryde A , Hershberger R , Chatonnet A , Patton MA , Crosby AH |
| Ref : American Journal of Human Genetics , 73 :1147 , 2003 |
| Abstract : Simpson_2003_Am.J.Hum.Genet_73_1147 |
| ESTHER : Simpson_2003_Am.J.Hum.Genet_73_1147 |
| PubMedSearch : Simpson_2003_Am.J.Hum.Genet_73_1147 |
| PubMedID: 14564668 |
| Gene_locus related to this paper: human-SPG21 |