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

Autor:	S. Alger, R. G. F. Gray, S. H. Green, A. Green, P. Davies
Rok vydání:	1999
Předmět:	Male medicine.medical_specialty LEBER HEREDITARY OPTIC NEUROPATHY X Chromosome Genetic Linkage DNA Mitochondrial Polymerase Chain Reaction Optic Atrophies Hereditary Internal medicine X-linked adrenoleukodystrophy Genetics medicine Humans Adrenoleukodystrophy Child Gene Genetics (clinical) Cells Cultured business.industry Fatty Acids Fibroblasts medicine.disease Phenotype Human genetics Endocrinology Mutation (genetic algorithm) Mutation business
Zdroj:	Journal of inherited metabolic disease. 22(6)
ISSN:	0141-8955
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b533a7118ee2881eb870424973ce7fd0 https://pubmed.ncbi.nlm.nih.gov/10472539 Zobrazit plný text záznamu Full text from SpringerLink Plný text