Haplotype analysis of spinocerebellar ataxia type 36 suggests a shared permissive core haplotype across populations
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Spinocerebellar ataxia type 36 (SCA36)-caused by a GGCCTG hexanucleotide repeat expansion in the NOP56 gene-has traditionally been considered to originate from a founder effect in the Ashida River basin of southern Japan. However, its genetic background remain... ...
