Publication | Open Access

Japanese Families with Autosomal Dominant Pure Cerebellar Ataxia Map to Chromosome 19p13.1-p13.2 and Are Strongly Associated with Mild CAG Expansions in the Spinocerebellar Ataxia Type 6 Gene in Chromosome 19p13.1

Mendelian DisorderGenetic DisorderGeneticsJapanese FamiliesMild Cag ExpansionsMolecular GeneticsDisease Gene IdentificationMedicineChromosome 19P13.1