Spinocerebellar Ataxia Type 8: Molecular Genetic Comparisonsand Haplotype Analysis of 37 Families with Ataxia

Author:

Ikeda Yoshio,Dalton Joline C.,Moseley Melinda L.,Gardner Kathy L.,Bird Thomas D.,Ashizawa Tetsuo,Seltzer William K.,Pandolfo Massimo,Milunsky Aubrey,Potter Nicholas T.,Shoji Mikio,Vincent John B.,Day John W.,Ranum Laura P.W.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference41 articles.

1. The KLHL1-antisense transcript (KLHL1AS) is evolutionarily conserved;Benzow;Mamm Genome,2002

2. Analysis of SCA8 and SCA12 loci in 134 Italian ataxic patients negative for SCA1-3, 6 and 7 CAG expansions;Brusco;J Neurol,2002

3. A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia;Cellini;Arch Neurol,2002

4. MRI studies in SCA8: cerebellar atrophy in unaffected expansion carriers partially explains reduced penetrance;Day;Am J Hum Genet,2003

5. Spinocerebellar ataxia type 8: clinical features in a large family;Day;Neurology,2000

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