Huntington disease: Difference between revisions
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Huntington disease (HD) is an [[autosomal dominant|autosomal dominant]] disorder that causes some of the nerve cells to degenerate<ref>NHS Choices,2012.Huntington's Disease (online) available at &amp;lt;http://www.nhs.uk/conditions/Huntingtons-disease/Pages/Introduction.aspx&amp;gt; (accessed 29th November 2013)</ref>. It caused by the mutation in HD [[gene|gene]] of [[chromosome 4|chromosome 4]].<ref>The university of UTAH, 2013. Genetic Scienc Learning Centre,(online) available at &amp;amp;lt;learn.genetic.utah.edu/content/disorders/whataregd/hunt/</ref> | |||
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Revision as of 02:37, 1 December 2013
Huntington disease (HD) is an autosomal dominant disorder that causes some of the nerve cells to degenerate[1]. It caused by the mutation in HD gene of chromosome 4.[2]
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- ↑ NHS Choices,2012.Huntington's Disease (online) available at &lt;http://www.nhs.uk/conditions/Huntingtons-disease/Pages/Introduction.aspx&gt; (accessed 29th November 2013)
- ↑ The university of UTAH, 2013. Genetic Scienc Learning Centre,(online) available at &amp;lt;learn.genetic.utah.edu/content/disorders/whataregd/hunt/