A Commom Disease Mechanism for Hereditary Neuropathies Due to Point Mutations in the Peripheral Myelin Protein 22 (ETH Diss. ; Nr. 13530)

A Commom Disease Mechanism for Hereditary Neuropathies Due to Point Mutations in the Peripheral Myelin Protein 22

(ETH Diss. ; Nr. 13530)

Name of awarding university/degree: Eidgenössische Technische Hochschule Zürich

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Material Type: 博士論文
Title: A Commom Disease Mechanism for Hereditary Neuropathies Due to Point Mutations in the Peripheral Myelin Protein 22
Author/Editor: Roland Naef.
Series Title: ETH Diss. ; Nr. 13530
Author Heading: Naef, Roland.
Publication, Distribution, etc.: Zürich : Eidgenössische Technische Hochschule Zürich
Publication Date: 2000.
Extent: 1 Microfiche ( 94 fr.) : negative, ill.
Degree grantor/type: Eidgenössische Technische Hochschule Zürich
Date Granted: 2000.
Date Granted (W3CDTF): 2000
Note (Dissertation): 博士論文
Thesis (doctoral) --Eidgenössische Technische Hochschule Zürich, 2000.
Place of Publication (Country Code): CH
Text Language Code: ger
Note (Material Type): [microform]
Note (General): Swiss Federal Institute of Technology.
Note (Bibliography): Includes bibliographies.
Summary in German and English.
Holding library: 国立国会図書館
Call No.: LS-DISE-13530
Data Provider (Database): 国立国会図書館 : 国立国会図書館蔵書
https://ndlsearch.ndl.go.jp
Bibliographic ID (NDL): 000003445120
http://id.ndl.go.jp/bib/000003445120
Bibliographic Record Category (NDL): 216