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A common disease mechanism for hereditary neuropathies due to point mutations in the peripheral myelin protein 22
| Metadata Label | Value |
|---|---|
| Autor(en): | Naef, Roland |
| Verlag: | Unbekannt |
| Zitierweise: | 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 |
| Dokumententyp: | Dissertationen und Habilitationen |
| Dokumente: |
Abstract
(420.33KB),
Fulltext
(7.54MB) |
Detailansicht
| Metadaten | Beschreibung |
|---|---|
| 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) | Neurowissenschaften |
| Keyword(s) |
MYELINPROTEINE NERVLICHE UND PSYCHIATRISCHE ERBKRANKHEITEN GENMUTATIONEN PUNKTMUTATIONEN GENETIK NEUROPLEXUS PERIPHERES NERVENSYSTEM NEUROPATHOLOGIE SCHWANN SCHE ZELLEN CYTOLOGIE HISTOLOGIE |
| Beschreibung | Dateiname | MIME Type | Grösse |
|---|---|---|---|
| Abstract |
eth-23419-01.pdf |
application/pdf | 420.33KB |
| Fulltext |
eth-23419-02.pdf |
application/pdf | 7.54MB |
| Beschreibung | URL |
|---|---|
| NEBIS Link | http://opac.nebis.ch/F/?local_base=NEBIS&func=find-b&find_code=SYS&request=003885341 |
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E-Collection record created: Fri, 18 Apr 2008, 21:59:40 CET