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Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.
Jørgen Erik Nielsen, B Johnson, Pernille Koefoed, K.H. Scheuer, M. Grønbech-Jensen, I. Law, K. Krabbe, Anne Nørremølle, Hans Rudolf Lytchoff Eiberg, H. Søndergård, M. Dam, J.F. Rehfeld, C. Krarup, O.B. Paulson, Lis Frydenreich Hasholt, Sven Asger Sørensen
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