Author:
Amorosi Cyntia Anabel,Myskóva Helena,Monti Mariela Roxana,Argaraña Carlos Enrique,Morita Masashi,Kemp Stephan,de Kremer Raquel Dodelson,Dvoráková Lenka,de Ramírez Ana María Oller
Publisher
Public Library of Science (PLoS)
Reference33 articles.
1. Incidence of X-linked adrenoleukodystrophy and the relative frequency of its phenotypes. Am J Med Genet;L Bezman,1998
2. ABCD1 mutation and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations;S Kemp;Hum Mutat,2001
3. Moser HW, Smith KD, Watkins PA, Powers J, Moser AB (2001) X-linked adrenoleukodystrophy. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds). The metabolic and molecular bases of inherited disease, ed. McGraw- Hill Inc, New York, 3257–3301.
4. Adrenoleukodystrophy: impaired oxidation of very long chain fatty acids in white blood cells, cultured skin fibroblasts, and amniocytes;I Singh;Pediatric Research,1984
5. Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls;AB Moser;Ann Neurol,1999
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