Mapping of a New Autosomal Dominant Spinocerebellar Ataxia to Chromosome 22

Author:

Zu Lan,Figueroa Karla P.,Grewal Raji,Pulst Stefan-M.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference27 articles.

1. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1;Benomar;Nat Genet,1995

2. A Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion;David;Nat Genet,1997

3. The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus;David;Am J Hum Genet,1996

4. Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion;Del-Favero;Hum Mol Genet,1998

5. Autosomal dominant spinocerebellar ataxia with sensory axonal (SCA4): clinical description and genetic localization to chromosome 16q22.1;Flanigan;Am J Hum Genet,1996

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