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

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

Open Access
|Nov 2008

References

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  2. 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.85.20.76472822493174658
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  4. 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/s00439990009010480364
  5. 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.122711748843
Language: English
Page range: 65 - 68
Published on: Nov 12, 2008
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 2008 S Grkovic, R Nikolic, M Djordjevic, Z Puzigaca, D Vujic, P Ilic, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons License.

Volume 11 (2008): Issue 1 (June 2008)