Huntington's disease - Revision history

170168250 at 17:13, 22 October 2018

2018-10-22T17:13:40Z

← Older revision		Revision as of 17:13, 22 October 2018
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	Huntington's disease is a genetic disorder, specifically affecting the [[~~gene~~ transcription\|gene]] that codes for the [[~~protein~~\|protein]] huntingtin<ref>J.M. Lee, E.M. Ramos, J.H. Lee, T. Gillis, J.S. Mysore, M.R. Hayden,S.C. Warby, P. Morrison, M. Nance, C.A. Ross, et al. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology. 2012 Mar 6; 78(10):690–695.</ref>. The symptoms of Huntington's disease include involuntary movements, depression, irritability and general behavioural changes<ref>S.C. Kirkwood,J.L. Su, P.M. Conneally, T Foroud. Progression of Symptoms in the Early and Middle Stages of Huntington Disease. Archives of Neurology.2001;58(2):273-278</ref>.		Huntington's disease is a genetic disorder, specifically affecting the [[Gene transcription\|gene]] that codes for the [[Protein\|protein]] huntingtin<ref>J.M. Lee, E.M. Ramos, J.H. Lee, T. Gillis, J.S. Mysore, M.R. Hayden,S.C. Warby, P. Morrison, M. Nance, C.A. Ross, et al. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology. 2012 Mar 6; 78(10):690–695.</ref>. The symptoms of Huntington's disease include involuntary movements, depression, irritability and general behavioural changes<ref>S.C. Kirkwood,J.L. Su, P.M. Conneally, T Foroud. Progression of Symptoms in the Early and Middle Stages of Huntington Disease. Archives of Neurology.2001;58(2):273-278</ref>.

			Huntingtons disease is an inhertied disease which causes areas of the brain to stop working overtime, and in many cases can becomes fatal after 20 years<ref>https://www.nhs.uk/conditions/huntingtons-disease/ (Accessed October 22, 2018)</ref>.

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Nnjm2: Cleaned up the pages. Added some links.

2016-12-06T21:18:12Z

Cleaned up the pages. Added some links.

← Older revision		Revision as of 21:18, 6 December 2016
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	Huntington's disease is a genetic disorder, specifically affecting the gene that codes for the protein huntingtin<ref>J.M. Lee, E.M. Ramos, J.H. Lee, T. Gillis, J.S. Mysore, M.R. Hayden,S.C. Warby, P. Morrison, M. Nance, C.A. Ross, et al. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology. 2012 Mar 6; 78(10):690–695.</ref>. The symptoms of Huntington's disease include involuntary movements, depression, irritability and general behavioural changes<ref>S.C. Kirkwood,J.L. Su, P.M. Conneally, T Foroud. Progression of Symptoms in the Early and Middle Stages of Huntington Disease. Archives of Neurology.2001;58(2):273-278</ref>.		Huntington's disease is a genetic disorder, specifically affecting the [[gene transcription\|gene]] that codes for the [[protein\|protein]] huntingtin<ref>J.M. Lee, E.M. Ramos, J.H. Lee, T. Gillis, J.S. Mysore, M.R. Hayden,S.C. Warby, P. Morrison, M. Nance, C.A. Ross, et al. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology. 2012 Mar 6; 78(10):690–695.</ref>. The symptoms of Huntington's disease include involuntary movements, depression, irritability and general behavioural changes<ref>S.C. Kirkwood,J.L. Su, P.M. Conneally, T Foroud. Progression of Symptoms in the Early and Middle Stages of Huntington Disease. Archives of Neurology.2001;58(2):273-278</ref>.

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2016-12-05T01:32:27Z

Created page with "Huntington's disease is a genetic disorder, specifically affecting the gene that codes for the protein huntingtin<ref>J.M. Lee, E.M. Ramos, J.H. Lee, T. Gillis, J.S. Mysore, M.R...."

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Huntington's disease is a genetic disorder, specifically affecting the gene that codes for the protein huntingtin<ref>J.M. Lee, E.M. Ramos, J.H. Lee, T. Gillis, J.S. Mysore, M.R. Hayden,S.C. Warby, P. Morrison, M. Nance, C.A. Ross, et al. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology. 2012 Mar 6; 78(10):690–695.</ref>. The symptoms of Huntington's disease include involuntary movements, depression, irritability and general behavioural changes<ref>S.C. Kirkwood,J.L. Su, P.M. Conneally, T Foroud. Progression of Symptoms in the Early and Middle Stages of Huntington Disease. Archives of Neurology.2001;58(2):273-278</ref>.

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