Mild overexpression of MeCP2 causes a progressive neurological disorder in mice-Reference-Cited by-同舟云学术

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Mild overexpression of MeCP2 causes a progressive neurological disorder in mice

Published:2004-09-06 Issue:21 Volume:13 Page:2679-2689
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Collins Ann L.,Levenson Jonathan M.,Vilaythong Alexander P.,Richman Ronald,Armstrong Dawna L.,Noebels Jeffrey L.,David Sweatt J.,Zoghbi Huda Y.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/13/21/2679/17241006/ddh282.pdf

Reference54 articles.

1. Hagberg, B., Aicardi, J., Dias, K. and Ramos, O. (1983) A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases. Ann. Neurol., 14, 471–479.

2. Amir, R.E., Van den Veyver, I.B., Wan, M., Tran, C.Q., Francke, U. and Zoghbi, H.Y. (1999) Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat. Genet., 23, 185–188.

3. Amir, R.E., Van den Veyver, I.B., Schultz, R., Malicki, D.M., Tran, C.Q., Dahle, E.J., Philippi, A., Timar, L., Percy, A.K., Motil, K.J. et al. (2000) Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes. Ann. Neurol., 47, 670–679.

4. Bienvenu, T., Carrie, A., de Roux, N., Vinet, M.C., Jonveaux, P., Couvert, P., Villard, L., Arzimanoglou, A., Beldjord, C., Fontes, M. et al. (2000) MECP2 mutations account for most cases of typical forms of Rett syndrome. Hum. Mol. Genet., 9, 1377–1384.

5. Auranen, M., Vanhala, R., Vosman, M., Levander, M., Varilo, T., Hietala, M., Riikonen, R., Peltonen, L. and Jarvela, I. (2001) MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features. Neurology, 56, 611–617.

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