NMDA receptor function in mouse models o
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Carlos Cepeda; Marjorie A. Ariano; Christopher R. Calvert; Jorge Flores-HernΓ‘nde
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Article
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2001
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John Wiley and Sons
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English
β 328 KB
## Abstract Huntington disease (HD) is an autosomal dominant disorder in which degeneration of mediumβsized spiny striatal neurons occurs. The HD gene and the protein it encodes, huntingtin, have been identified but their functions remain unknown. Transgenic mouse models for HD have been developed