| 摘要 |
<p>The present invention relates to a diagnosis method for a multiplication disease of repeated trinucleotide sequences and a diagnosis kit, and more particularly to a method for diagnosing Huntington disease, Kennedy disease, Spinocerabellar ataxia type 1, Spinocerebellar ataxia type 2, Spinocerebellar ataxia type 3, Spinocerebellar ataxia type 6, Spinocerebellar ataxia type 7, Dentatorubral-pallidoluysian atrophy, Fragile X syndrome, Fragile E site, Myotonic dystrophy, Friedreich ataxia or Spinocerebellar ataxia type 8 by micro capillary electrophoresis,and thereby patients and silent carriers having a multiplication disease of repeated trinucleotide sequences can be easily detected.</p> |
