| 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 |
| Gene_locus related to this paper: human-SPG21 |
Simpson MA, Cross H, Proukakis C, Pryde A, Hershberger R, Chatonnet A, Patton MA, Crosby AH (2003)
Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia
American Journal of Human Genetics
73 :1147
Simpson MA, Cross H, Proukakis C, Pryde A, Hershberger R, Chatonnet A, Patton MA, Crosby AH (2003)
American Journal of Human Genetics
73 :1147