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The Leber hereditary optic neuropathy 14484 mutation and X-linked adrenoleukodystrophy: A possible modifier of phenotypic expression?

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Journal of Inherited Metabolic Disease

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References

  • Funalot B, Ranoux D, Mas J-L, Garcia C, Bonnefont J-P (1996) Brainstem involvement in Leber's hereditary optic neuropathy: association with the 14484 mitochondrial mutation. J Neurol Neurosurg Psychiatry 61: 533-534.

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  • Moser HW (1997) Adrenoleukodystrophy: phenotype, genetics, pathogenesis and therapy. Brain 120: 1485-1508.

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  • Traboulsi EI and Maumenee IH (1987) Ophthalmological manifestations of X-linked childhood adrenoleukodystrophy. Ophthalmology 94: 47-52.

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Authors and Affiliations

  1. Department of Clinical Chemistry, Diana Princess of Wales Children's Hospital, Steelhouse Lane, Birmingham, B4 6NH, UK

    R. G. F. Gray, P. Davies, S. Alger & A. Green

  2. Department of Neurology, Diana Princess of Wales Children's Hospital, Steelhouse Lane, Birmingham, B4 6NH, UK

    S. H. Green

Authors
  1. R. G. F. Gray
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  2. S. H. Green
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  3. P. Davies
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  4. S. Alger
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  5. A. Green
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Gray, R.G.F., Green, S.H., Davies, P. et al. The Leber hereditary optic neuropathy 14484 mutation and X-linked adrenoleukodystrophy: A possible modifier of phenotypic expression?. J Inherit Metab Dis 22, 760–761 (1999). https://doi.org/10.1023/A:1005520922737

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  • DOI: https://doi.org/10.1023/A:1005520922737

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