A common disease mechanism for hereditary neuropathies due to point mutations in the peripheral myelin protein 22

Metadata Label Value
Author(s): Naef, Roland
Publisher: Unknown
Citation:

Naef, Roland. A common disease mechanism for hereditary neuropathies due to point mutations in the peripheral myelin protein 22. (2000). http://dx.doi.org/10.3929/ethz-a-003885341

Document Type: Doctoral and Habilitation Theses  
Documents: Abstract (420.33KB) , Fulltext (7.54MB)
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Metadata Description
Title A common disease mechanism for hereditary neuropathies due to point mutations in the peripheral myelin protein 22
Author(s) Naef, Roland
Publication Place Zürich
Publication Date 2000
Notes Diss. Naturwissenschaften ETH Zürich, Nr. 13530, 2000
Language English
DOI http://dx.doi.org/10.3929/ethz-a-003885341
Subject(s) Neurosciences
Keyword(s) MYELIN PROTEINS
HEREDITARY NERVOUS AND PSYCHIATRIC DISORDERS
GENE MUTATIONS
POINT MUTATIONS
GENETICS
PERIHERAL NERVOUS SYSTEM
NEUROPATHOLOGY
SCHWANN CELLS
CYTOLOGY AND HISTOLOGY
Description File Name MIME Type Size
Abstract   eth-23419-01.pdf application/pdf 420.33KB
Fulltext   eth-23419-02.pdf application/pdf 7.54MB
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E-Collection record created: Fri, 18 Apr 2008, 21:59:40 CET