A Novel Mutation of the ABCD1 Gene in Serbian X-Adrenoleukodystrophy

Moser W, Smith D, Watkins A, Powers J, Moser B. X-linked adrenoleukodystrophy. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Eds. The Metabolic and Molecular Bases of Inherited Disease, 8th ed. New York: McGraw-Hill. 2001; 3257-3301.Search in Google Scholar

Lazo O, Contreras M, Hashmi M, Stanley W, Irazu C, Singh I. Peroxisomal lignoceroyl-CoA ligase deficiency in childhood adrenoleukodystrophy and adrenomyeloneuropathy. Proc Natl Acad Sci USA 1988; 85(5): 7647-7651.10.1073/pnas.85.20.76472822493174658Search in Google Scholar

Mathew CC. The isolation of high molecular weight eukaryotic DNA. In: Walker JM, Ed. Methods in Molecular Biology, Vol. 11. New York: Human Press. 1984; 31-34.10.1385/0-89603-064-4:31Search in Google Scholar

Wichers M, Kohler W, Brennemann W, Boese V, Sokolowski P, Bidlingmaier F, Ludwig M. X-linked adrenoleukodystrophy associated with 14 novel ALD gene mutations: no correlation between type of mutation and age of onset. Hum Genet 1999; 105(2?): 116-119.10.1007/s00439990009010480364Search in Google Scholar

Kemp S, Pujol A, Waterham HR, van Geel BM, Boehm CD, Raymond GV, Cutting GR, Wanders RJ, Moser HW. ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations. Hum Mutat 2001; 18(3): 499-515.10.1002/humu.122711748843Search in Google Scholar