Diagnostic copper imaging of Menkes disease by synchrotron radiation-generated X-ray fluorescence analysis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep33247.pdf
Reference30 articles.
1. Kodama, H., Fujisawa, C. & Bhadhprasit, W. Inherited copper transport disorders: Biochemical mechanisms, diagnosis, and treatment. Curr. Drug. Metab. 13, 237–250 (2012).
2. Bie, P. D., Muller, P., Wijmenga, C. & Klomp, L. W. J. Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes. J. Med. Genet. 44, 673–688 (2007).
3. Gupta, A. & Lutsenko, S. Human coppertransporters: mechanism, role in human diseases and therapeutic potential. Future. Med. Chem. 1, 1125–1142 (2009).
4. Sarkar, B., Lingertat-Walsh, K. & Clarke, J. T. Copper-histidine therapy for Menkes disease. J. Pediatr. 123, 828–830 (1993).
5. Sarkar, B. Treatment of Wilson and menkes diseases. Chem. Rev. 99, 2535–2544 (1999).
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