Carrier identification of X-linked adrenoleukodystrophy by measurement of very long chain fatty acids and lignoceric acid oxidation
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1996.tb02386.x/fullpdf
Reference24 articles.
1. Linkage of adrenoleukodystrophy to a polymorphic DNA probe;Aubourg;Ann Neurol,1987
2. Morbus Addison mit Himsklerose im Kindesalter. Ein Hereditares Syndrom mit X-chromosomaler Vererbung;Fanconi;Helv Paediatr Acta,1963
3. Lignoceroyl-CoASH ligase: enzyme defect in fatty acid beta oxidation system in X-linked childhood adrenoleukodystrophy;Hashmi;FEBS Lett,1986
4. Fatty acid abnormality in adrenoleukodystrophy;Igarashi;J Neurochem,1976
5. Conclusive evidence that very-longchain fatty acids are oxidized exclusively in peroxisomes in human skin fibroblasts;Jakobs;Biochem Biophys Res Commun,1991
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