Author:
Skjørringe Tina,Amstrup Pedersen Per,Salling Thorborg Sidsel,Nissen Poul,Gourdon Pontus,Birk Møller Lisbeth
Publisher
Springer Science and Business Media LLC
Reference55 articles.
1. Tumer, Z. & Moller, L. B. Menkes disease. Eur. J. Hum. Genet. 18, 511–518 (2010).
2. Menkes, J. H., Alter, M. & Steigleder, G. K. et al. A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration. Pediatrics 29, 764–779 (1962).
3. Lenartowicz, M., Krzeptowski, W., Koteja, P., Chrzascik, K. & Møller, L. B. Prenatal Treatment of Mosaic Mice (Atp7a mo-ms) Mouse Model for Menkes Disease, with Copper Combined by Dimethyldithiocarbamate (DMDTC). PLoS One. 7, e40400 (2012).
4. Kennerson, M. L. et al. Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy. Am J Hum Genet 86, 343–52, doi: 10.1016/j.ajhg.2010.01.027 (2010).
5. Gourdon, P., Liu, X. Y., Skjorringe, T., Morth, J. P., Moller, L. B., Pedersen, B. P. & Nissen, P. Crystal structure of a copper-transporting PIB-type ATPase. Nature 475, 59–64 (2011).
Cited by
35 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献