Wilson's disease - Revision history

Nnjm2 at 18:04, 2 December 2015

2015-12-02T18:04:55Z

← Older revision		Revision as of 18:04, 2 December 2015
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	Wilson disease is an inheritable autosomal [~~https://teaching.ncl.ac.uk/bms/wiki/index.php/Autosomal_recessive_disease~~ recessive disorder ]and is a result of mutations in the APT7B gene. The APT7B gene encodes a protein required to remove surplus copper from the body, [[Mutations\|mutations]] in this gene reduce the functionality of the transport protein resulting in harmful accumulation of copper in the body [http://ghr.nlm.nih.gov/condition/wilson-disease ~~http://ghr.nlm.nih.gov~~/~~condition/wilson-disease]~~.		Wilson disease is an inheritable autosomal [[Recessive_disorder\|recessive disorder]] and is a result of mutations in the [[APT7B gene\|APT7B gene]]. The APT7B gene encodes a [[protein\|protein]] required to remove surplus [[copper\|copper]] from the body, [[Mutations\|mutations]] in this gene reduce the functionality of the transport protein resulting in harmful accumulation of copper in the body<ref>http://ghr.nlm.nih.gov/condition/wilson-disease</ref>.

			=== Reference ===

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150005467 at 17:28, 2 December 2015

2015-12-02T17:28:07Z

← Older revision		Revision as of 17:28, 2 December 2015
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	Wilson disease is an inheritable autosomal [https://teaching.ncl.ac.uk/bms/wiki/index.php/Autosomal_recessive_disease recessive disorder ]and is a result of mutations in the APT7B gene. The APT7B gene encodes a protein required to remove surplus copper from the body, mutations in this gene reduce the functionality of the transport protein resulting in harmful accumulation of copper in the body [http://ghr.nlm.nih.gov/condition/wilson-disease http://ghr.nlm.nih.gov/condition/wilson-disease].		Wilson disease is an inheritable autosomal [https://teaching.ncl.ac.uk/bms/wiki/index.php/Autosomal_recessive_disease recessive disorder ]and is a result of mutations in the APT7B gene. The APT7B gene encodes a protein required to remove surplus copper from the body, [[Mutations\|mutations]] in this gene reduce the functionality of the transport protein resulting in harmful accumulation of copper in the body [http://ghr.nlm.nih.gov/condition/wilson-disease http://ghr.nlm.nih.gov/condition/wilson-disease].

130601874: Created page with "Wilson disease is an inheritable autosomal [https://teaching.ncl.ac.uk/bms/wiki/index.php/Autosomal_recessive_disease recessive disorder ]and is a result of mutations in the APT7..."

2013-11-15T12:38:06Z

Created page with "Wilson disease is an inheritable autosomal [https://teaching.ncl.ac.uk/bms/wiki/index.php/Autosomal_recessive_disease recessive disorder ]and is a result of mutations in the APT7..."

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Wilson disease is an inheritable autosomal [https://teaching.ncl.ac.uk/bms/wiki/index.php/Autosomal_recessive_disease recessive disorder ]and is a result of mutations in the APT7B gene. The APT7B gene encodes a protein required to remove surplus copper from the body, mutations in this gene reduce the functionality of the transport protein resulting in harmful accumulation of copper in the body [http://ghr.nlm.nih.gov/condition/wilson-disease http://ghr.nlm.nih.gov/condition/wilson-disease]. 