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  Genetische Defekte der Myelinbildung: Molekulare Pathogenese der Charcot-Marie-Tooth Neuropathie (CMT1A)

Meyer zu Hörste, G., & Sereda, M. W. (2005). Genetische Defekte der Myelinbildung: Molekulare Pathogenese der Charcot-Marie-Tooth Neuropathie (CMT1A). Neuroforum, 1, 25-30. doi:10.1515/nf-2005-0105.

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10.1515_nf-2005-0105.pdf (Publisher version), 191KB
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10.1515_nf-2005-0105.pdf
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 Creators:
Meyer zu Hörste, Gerd1, Author           
Sereda, Michael W.1, Author           
Affiliations:
1Molecular and translational neurology, Neurogenetics, Max Planck Institute of Experimental Medicine, Max Planck Society, ou_2173667              

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Language(s): deu - German
 Dates: 2005
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1515/nf-2005-0105
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Title: Neuroforum
Source Genre: Journal
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Pages: - Volume / Issue: 1 Sequence Number: - Start / End Page: 25 - 30 Identifier: ISSN: 0947-0875
CoNE: https://pure.mpg.de/cone/journals/resource/110978984249776