Leber's Hereditary Optic Neuropathy

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(Created page with "Leber's hereditary optic neuropathy is a mitochondrial disease caused by 1 of 3 mutations in mtDNA; G11778A, T14484C or G3460A, in the ND1, ND4, ND4L or ND6 genes of mitochondria...")
 
 
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Leber's hereditary optic neuropathy is a mitochondrial disease caused by 1 of 3 mutations in mtDNA; G11778A, T14484C or G3460A, in the ND1, ND4, ND4L or ND6 genes of mitochondrial DNA<ref name="US GHR Website">This is in reference to the website https://ghr.nlm.nih.gov/condition/leber-hereditary-optic-neuropathy#genes
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Leber's hereditary [[optic neuropathy|optic neuropathy]] is a [[mitochondrial disease|mitochondrial disease]] caused by 1 of 3 mutations in [[mtDNA|mtDNA]]; G11778A, T14484C or G3460A, in the ND1, ND4, ND4L or ND6 genes of [[mitochondrial DNA|mitochondrial DNA]]<ref name="US GHR Website">This is in reference to the website https://ghr.nlm.nih.gov/condition/leber-hereditary-optic-neuropathy#genes Cited on 3/12/18.</ref>.<ref name="Eye Wiki Website">This is also in reference to the Eye Wiki website, http://eyewiki.aao.org/Leber_Hereditary_Optic_Neuropathy Cited on 3/12/18</ref>.  
Cited on 3/12/18.</ref><ref name="Eye Wiki Website">This is also in reference to the Eye Wiki website, http://eyewiki.aao.org/Leber_Hereditary_Optic_Neuropathy
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Cited on 3/12/18</ref>.
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=== References ===
 
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<u>References</u>
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Latest revision as of 14:49, 3 December 2018

Leber's hereditary optic neuropathy is a mitochondrial disease caused by 1 of 3 mutations in mtDNA; G11778A, T14484C or G3460A, in the ND1, ND4, ND4L or ND6 genes of mitochondrial DNA[1].[2].

References

  1. This is in reference to the website https://ghr.nlm.nih.gov/condition/leber-hereditary-optic-neuropathy#genes Cited on 3/12/18.
  2. This is also in reference to the Eye Wiki website, http://eyewiki.aao.org/Leber_Hereditary_Optic_Neuropathy Cited on 3/12/18
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