Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.

Nielsen, J E; Johnsen, B; Koefoed, P; Scheuer, K H; Grønbech-Jensen, M; Law, I; Krabbe, K; Nørremølle, A; Eiberg, H; Søndergård, H; Dam, M; Rehfeld, J F; Krarup, C; Paulson, O B; Hasholt, L; Sørensen, S A

Nielsen, J E; Johnsen, B; Koefoed, P; Scheuer, K H; Grønbech-Jensen, M; Law, I; Krabbe, K; Nørremølle, A; Eiberg, H; Søndergård, H; Dam, M; Rehfeld, J F; Krarup, C; Paulson, O B; Hasholt, L; Sørensen, S A.

Affiliation

Nielsen JE; Department of Medical Genetics, Institute of Medical Biochemistry and Genetics, University of Copenhagen, Copenhagen, Denmark. jnielsen@imbg.ku.dk

Eur J Neurol ; 11(12): 817-24, 2004 Dec.

Article in En | MEDLINE | ID: mdl-15667412

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Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Spastic Paraplegia, Hereditary / Cerebellar Ataxia / Adenosine Triphosphatases / Mutation Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2004 Document type: Article Affiliation country: Dinamarca Country of publication: Reino Unido

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