Title : Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.

Pub. Date : 1997 Feb

PMID : 9020849






1 Functional Relationships(s)
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Protein Name
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1 Six inherited neurodegenerative diseases are caused by a CAG/polyglutamine expansion, including spinal and bulbar muscular atrophy (SBMA), Huntington"s disease (HD), spinocerebellar ataxia type 1 (SCA1), dentatorubral pallidoluysian atrophy (DRPLA) Machado-Joseph disease (MJD or SCA3) and SCA2. polyglutamine atrophin 1 Mus musculus