Autosomal dominant spinocerebellar ataxias ad infinitum?

Neurology

Volumn 56, Issue 3, 2001, Pages 287-289

  Subramony, S H ^a   Filla, A ^b  

^a UNIVERSITY OF MISSISSIPPI SCHOOL OF MEDICINE   (United States)

^b Clinica Neurologia   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT DISORDER; CLINICAL FEATURE; DIAGNOSTIC PROCEDURE; DISEASE CLASSIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; GENOTYPE; HUMAN; PHENOTYPE; POPULATION GENETICS; PRIORITY JOURNAL; REVIEW; SPINOCEREBELLAR DEGENERATION;

EID: 0035852807     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.56.3.287     Document Type: Review

References (14)

1. Spinocerebellar ataxia type 12 (SCA 12): Clinical and neuroradiologic features
2. Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA 12
3. Spinocerebellar ataxia type 12 is rare in the United Kingdom
4. Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically determined subtypes?
5. Autosomal dominant spinocere-bellar ataxia with sensory axonal neuropathy (SCA 4): Clinical description and genetic localization to chromosome 16q22.1
6. Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11
7. Autosomal dominant cerebellar ataxia (SCA 6) associated with small polyglutamine expansion in the alpha 1A-voltage-dependent calcium channel
8. Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SAC 7)
9. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA 8)
10. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
11. Autosomal dominant cerebellar ataxia type III: Linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3
12. Mapping of the spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation
13. A novel locus for dominant cerebellar ataxia (SCA 14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter
14. A novel type of autosomal dominant cerebellar ataxia linked to chromosome 8q