Report for Pryde A

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References (1)

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