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The-LHON-Enigma: explaining the behaviour of Leber’s Hereditary Optic Neuropathy by the use of a simple computer model

bioRxiv

Nov 25, 2013

Ian S Logan

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Abstract

Leber?s Hereditary Optic Neuropathy (LHON) appears as an enigmatic condition; affecting only certain families and often causing a severe loss of vision seemingly at random amongst family members. The first breakthrough came in 1988 with the linking of the condition to a mutation in the ...read more

Mentioned in this Paper

Nadh Dehydrogenase Complex
Mutation Abnormality
Mitochondrial DNA Location
Unspecified Visual Loss
Mitochondria
Sciurus oculatus
PDLIM7 gene
DNA, Mitochondrial
Optic Atrophy, Hereditary, Leber
Vision
1
2
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  • The-LHON-Enigma: explaining the behaviour of Leber’s Hereditary Optic Neuropathy by the use of a simple computer model

    bioRxiv

    Nov 25, 2013

    Ian S Logan

    PMID: 990000935

    DOI: 10.1101/000935

    Abstract

    Leber?s Hereditary Optic Neuropathy (LHON) appears as an enigmatic condition; affecting only certain families and often causing a severe loss of vision seemingly at random amongst family members. The first breakthrough came in 1988 with the linking of the condition to a mutation in the ...read more

    Mentioned in this Paper

    Nadh Dehydrogenase Complex
    Mutation Abnormality
    Mitochondrial DNA Location
    Unspecified Visual Loss
    Mitochondria
    1
    2

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