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  Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations.

Brockmann, K., Dreha-Kulaczewski, S., Dechent, P., Bonnemann, C., Helms, G., Kyllermann, M., et al. (2008). Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations. Journal of Neurology, 255(7): DOI: 10.1007/s00415-008-0847-1, pp. 1049-1058. Retrieved from http://www.springerlink.com/content/0175p4p845245ql6/fulltext.pdf.

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Brockmann, K., Author
Dreha-Kulaczewski, S., Author
Dechent, P.1, Author           
Bonnemann, C., Author
Helms, G., Author
Kyllermann, M., Author
Brueck, W., Author
Frahm, J.1, Author           
Huehne, K., Author
Gaertner, J., Author
Rautenstrauss, B., Author
Affiliations:
1Biomedical NMR Research GmbH, MPI for biophysical chemistry, Max Planck Society, ou_578634              

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Free keywords: hereditary motor and sensory neuropathy; Charcot-Marie-Tooth disease; mitofusin; macrocephaly; magnetic resonance spectroscopy
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Language(s): eng - English
 Dates: 2008-07
 Publication Status: Issued
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Title: Journal of Neurology
Source Genre: Journal
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Pages: - Volume / Issue: 255 (7) Sequence Number: DOI: 10.1007/s00415-008-0847-1 Start / End Page: 1049 - 1058 Identifier: -