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

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Bibliographic Details
Published inJournal of inherited metabolic disease Vol. 22; no. 6; pp. 760 - 761
Main Authors Gray, R. G. F., Green, S. H., Davies, P., Alger, S., Green, A.
Format Journal Article
LanguageEnglish
Published Dordrecht Kluwer Academic Publishers 01.08.1999
Springer
Blackwell Publishing Ltd
Subjects
Biological and medical sciences
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Medical sciences
Neurology
Endocrinopathy
Human
Nervous system diseases
Clinical form
Metabolic diseases
Lipids
Enzymopathy
Cerebral disorder
Genetic disease
Case study
Symptomatology
Adrenoleukodystrophy
Association
Gene
Adrenal gland diseases
Leber optic neuropathy
Mutation
Child
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More Information
ISSN:0141-8955
1573-2665
DOI:10.1023/A:1005520922737