Literature DB >> 10472539

The Leber hereditary optic neuropathy 14,484 mutation and X-linked adrenoleukodystrophy: a possible modifier of phenotypic expression?

R G Gray1, S H Green, P Davies, S Alger, A Green.   

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Year:  1999        PMID： 10472539     DOI： 10.1023/a:1005520922737

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  3 in total

Review 1.  Adrenoleukodystrophy: phenotype, genetics, pathogenesis and therapy.

Authors:  H W Moser
Journal:  Brain       Date:  1997-08       Impact factor: 13.501

2.  Brainstem involvement in Leber's hereditary optic neuropathy: association with the 14,484 mitochondrial DNA mutation.

Authors:  B Funalot; D Ranoux; J L Mas; C Garcia; J P Bonnefont
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-11       Impact factor: 10.154

3.  Ophthalmologic manifestations of X-linked childhood adrenoleukodystrophy.

Authors:  E I Traboulsi; I H Maumenee
Journal:  Ophthalmology       Date:  1987-01       Impact factor: 12.079
  3 in total

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