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Polyglutamine (polyQ) disorders

  • Cohen-Carmon D
  • Meshorer E
Nucleus (2012) 3(5) 433-441
DOI: 10.4161/nucl.21481
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Abstract

Polyglutamine-expansion disease family encompasses at least nine heritable disorders, including Huntington disease (HD) and the spinocerebellar ataxias SCA1, SCA2, SCA3, SCA6, SCA7 and SCA17 (revie...

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Cohen-Carmon, D., & Meshorer, E. (2012). Polyglutamine (polyQ) disorders. Nucleus, 3(5), 433–441. https://doi.org/10.4161/nucl.21481

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