Huntington disease: Difference between revisions
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Huntington disease (HD) is an [[ | 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;amp;amp;amp;lt;http://www.nhs.uk/conditions/Huntingtons-disease/Pages/Introduction.aspx&amp;amp;amp;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 http://learn.genetic.utah.edu/content/disorders/whataregd/hunt/</ref>. | ||
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Revision as of 02:38, 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].
References
- ↑ NHS Choices,2012.Huntington's Disease (online) available at &amp;amp;amp;lt;http://www.nhs.uk/conditions/Huntingtons-disease/Pages/Introduction.aspx&amp;amp;amp;gt; (accessed 29th November 2013)
- ↑ The university of UTAH, 2013. Genetic Scienc Learning Centre,(online) available at http://learn.genetic.utah.edu/content/disorders/whataregd/hunt/