Adrenoleukodystrophy: diagnosis and carrier detection by determination of long-chain fatty acids in cultured fibroblasts
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1982.tb01406.x/fullpdf
Reference14 articles.
1. Addison disease and cerebral sclerosis in an apparently heterozygous girl: evidence for inactiv-ation of the adrenoleukodystrophy locus;Heffungs;Clin. Genet.,1980
2. Fatty acid abnormality in adrenoleukodystrophy;Igarashi;J. Neurochem.,1976
3. High concentration of hexacosaonate in cultured skin fibroblast lipids from adrenoleukodystrophy patients;Kawamura;Biochem. Biophys. Res. Commun.,1978
4. Adrenoleukodystrophy: Evidence for X linkage, inactiv-ation and selection favoring the mutant allele in heterozygous cells;Migeon;Proc. nat. Acad. Sci. (Wash.),1981
5. Adrenoleukodystrophy: elevated C26 fatty acid in cultured skin fibroblasts;Moser;Ann. Neurol.,1980
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