Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family.

Filla, A; De Michele, G; Banfi, S; Santoro, L; Perretti, A; Cavalcanti, F; Pianese, L; Castaldo, I; Barbieri, F; Campanella, G

Filla, A; De Michele, G; Banfi, S; Santoro, L; Perretti, A; Cavalcanti, F; Pianese, L; Castaldo, I; Barbieri, F; Campanella, G.

Affiliation

Filla A; Department of Neurology, Federico II University, Naples, Italy.

Neurology ; 45(4): 793-6, 1995 Apr.

Article in En | MEDLINE | ID: mdl-7723972

Subject(s)

Spinocerebellar Degenerations/genetics; Adult; Aged; Chromosomes, Human, Pair 12; DNA/analysis; Female; Genetic Linkage; Haplotypes; Humans; Italy; Male; Middle Aged; Phenotype; Polymerase Chain Reaction

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Collection: 01-internacional Database: MEDLINE Main subject: Spinocerebellar Degenerations Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Neurology Year: 1995 Document type: Article

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