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Huntington s disease (HD) is an autosomal dominant neurodegenerative ...

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Topic: Huntington
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Sort Desciption: Huntingtons disease (HD) is a dominant neurodegenerative disorder caused by expansion of a CAG trinucleotide repeat in the HD gene from about 6-35 repeats (non-HD range) to 36-100 repeats (HD range), extending a normally variable run of glutamines in the huntingtin protein. ...

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Huntingtons disease (HD) is a dominant neurodegenerative disorder caused by expansion of a CAG trinucleotide repeat in the HD gene from about 6-35 repeats (non-HD range) to 36-100 repeats (HD range), extending a normally variable run of glutamines in the huntingtin protein. We have established genetic criteria from studies of human patients that define characteristics of the trigger mechanism (dominance, increasing severity with increased polyglutamine tract length in the non-HD and the HD range) but the biochemical ...

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