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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.1988; 85(5): 7647-7651.
  3. Mathew CC. The isolation of high molecular weight eukaryotic DNA. In: Walker JM, Ed., Vol. 11. New York: Human Press. 1984; 31-34.
  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.1999; 105(2?): 116-119.
  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.2001; 18(3): 499-515.
DOI: https://doi.org/10.2478/v10034-008-0020-2 | Journal eISSN: 2199-5761 (formerly 1311-0160) | Journal ISSN: 1311-0160
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

© 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.