Adrenoleukodystrophy – neuroendocrine pathogenesis and redefinition of natural history-Reference-Cited by-同舟云学术

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Adrenoleukodystrophy – neuroendocrine pathogenesis and redefinition of natural history

Published:2016-06-17 Issue:10 Volume:12 Page:606-615
ISSN:1759-5029
Container-title:Nature Reviews Endocrinology
language:en
Short-container-title:Nat Rev Endocrinol

Author:

Kemp Stephan,Huffnagel Irene C.,Linthorst Gabor E.,Wanders Ronald J.,Engelen Marc

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.nature.com/articles/nrendo.2016.90.pdf

Reference148 articles.

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2. Argmann, C. A., Houten, S. M., Zhu, J. & Schadt, E. E. A. Next generation multiscale view of inborn errors of metabolism. Cell Metab. 23, 13–26 (2016).

3. Mosser, J. et al. Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters. Nature 361, 726–730 (1993).

4. Singh, I., Moser, A. E., Moser, H. W. & Kishimoto, Y. Adrenoleukodystrophy: impaired oxidation of very long chain fatty acids in white blood cells, cultured skin fibroblasts, and amniocytes. Pediatr. Res. 18, 286–290 (1984).

5. Wanders, R. J. et al. Peroxisomal very long-chain fatty acid β-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders. Clin. Chim. Acta 166, 255–263 (1987).

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