A common disease mechanism for hereditary neuropathies due to point mutations in the peripheral myelin protein 22
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Author
Date
2000Type
- Doctoral Thesis
ETH Bibliography
yes
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Permanent link
https://doi.org/10.3929/ethz-a-003885341Publication status
publishedExternal links
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Publisher
ETH ZürichSubject
MYELINPROTEINE; GENMUTATIONEN + PUNKTMUTATIONEN (GENETIK); NEUROPLEXUS + PERIPHERES NERVENSYSTEM (NEUROPATHOLOGIE); NERVLICHE UND PSYCHIATRISCHE ERBKRANKHEITEN; SCHWANN'SCHE ZELLEN (CYTOLOGIE, HISTOLOGIE); MYELIN PROTEINS; GENE MUTATIONS + POINT MUTATIONS (GENETICS); NEUROPLEXUS + PERIHERAL NERVOUS SYSTEM (NEUROPATHOLOGY); HEREDITARY NERVOUS AND PSYCHIATRIC DISORDERS; SCHWANN CELLS (CYTOLOGY, HISTOLOGY)Organisational unit
03367 - Suter, Ulrich / Suter, Ulrich
Notes
Diss. Naturwissenschaften ETH Zürich, Nr. 13530, 2000.More
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ETH Bibliography
yes
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