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Paper Report for: Simpson_2003_Am.J.Hum.Genet_73_1147

Reference
Title: Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia
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 : PubMed

        


Related information
Gene_Locus : human-SPG21
Mutation : T201NfsX11_human-SPG21,

Citations formats
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: 1147-56

Simpson MA, Cross H, Proukakis C, Pryde A, Hershberger R, Chatonnet A, Patton MA, Crosby AH (2003)
American Journal of Human Genetics 73: 1147-56


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