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“Novel exon nucleotide deletion causes adrenoleukodystrophy in a Brazilian family”, vol. 10, pp. 65-74, 2011.
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http://dx.doi.org/10.1016/j.braindev.2009.02.002
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Kemp S and Wanders RJ (2007). X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism, ABC half-transporters and the complicated route to treatment. Mol. Genet. Metab. 90: 268-276.
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Lachtermacher MB, Seuanez HN, Moser AB, Moser HW, et al. (2000). Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously described. Hum. Mutat. 15: 348-353.
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Mahmood A, Dubey P, Moser HW and Moser A (2005). X-linked adrenoleukodystrophy: therapeutic approaches to distinct phenotypes. Pediatr. Transplant. 9 (Suppl 7): 55-62.
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Montagna G, Di Biase A, Cappa M, Melone MA, et al. (2005). Identification of seven novel mutations in ABCD1 by a DHPLC-based assay in Italian patients with X-linked adrenoleukodystrophy. Hum. Mutat. 25: 222.
http://dx.doi.org/10.1002/humu.9303
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Moser HW (2006). Therapy of X-linked adrenoleukodystrophy. NeuroRx 3: 246-253.
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