Recent advances in hereditary spastic paraplegia.

Tallaksen, C M; Dürr, A; Brice, A

Tallaksen, C M; Dürr, A; Brice, A.

Affiliation

Tallaksen CM; INSERM U289, Département de Génétique, Cytogénétique et Embryologie, et Fédération de Neurologie, Hôpital de la Salpêtrière, Paris, France.

Curr Opin Neurol ; 14(4): 457-63, 2001 Aug.

Article in En | MEDLINE | ID: mdl-11470961

Subject(s)

Spastic Paraplegia, Hereditary/genetics; Chromosome Aberrations/genetics; Chromosome Disorders; Chromosome Mapping; Genes, Dominant/genetics; Genes, Recessive/genetics; Genetic Predisposition to Disease/genetics; Humans; Phenotype; Sex Chromosome Aberrations/genetics; Spastic Paraplegia, Hereditary/classification; Spastic Paraplegia, Hereditary/diagnosis; X Chromosome

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Curr Opin Neurol Journal subject: NEUROLOGIA Year: 2001 Document type: Article Affiliation country: France Country of publication: United kingdom

Search on Google

Add to My VHL

XML

PubMed Links