Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.

Mrissa, N; Belal, S; Hamida, C B; Amouri, R; Turki, I; Mrissa, R; Hamida, M B; Hentati, F

Mrissa, N; Belal, S; Hamida, C B; Amouri, R; Turki, I; Mrissa, R; Hamida, M B; Hentati, F.

Affiliation

Mrissa N; Institut National de Neurologie, Tunis, Tunisia.

Neurology ; 54(7): 1408-14, 2000 Apr 11.

Article in En | MEDLINE | ID: mdl-10751248

Subject(s)

Chromosomes, Human, Pair 13/genetics; Genetic Linkage/genetics; Spinocerebellar Degenerations/genetics; Adolescent; Adult; Age of Onset; Biopsy; Evoked Potentials, Somatosensory/genetics; Female; Genes, Recessive/genetics; Genetic Markers; Humans; Lod Score; Magnetic Resonance Angiography; Male; Middle Aged; Muscle, Skeletal/innervation; Muscle, Skeletal/pathology; Neural Conduction/genetics; Pedigree; Peroneal Nerve/pathology; Spinocerebellar Degenerations/epidemiology; Tunisia/epidemiology

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Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 13 / Spinocerebellar Degenerations / Genetic Linkage Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Country/Region as subject: Africa Language: En Journal: Neurology Year: 2000 Type: Article Affiliation country: Tunisia

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