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  TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome.

Hoffmann, L. A., Lohse, P., König, F. B., Feneberg, W., Hohlfeld, R., & Kümpfel, T. (2008). TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome. Neurology, 70(13 Pt 2), 1155-1156.

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 Creators:
Hoffmann, L. A.1, Author           
Lohse, P., Author
König, F. B., Author
Feneberg, W., Author
Hohlfeld, R.1, Author           
Kümpfel, T.1, Author           
Affiliations:
1Department: Neuroimmunology / Wekerle, MPI of Neurobiology, Max Planck Society, ou_1113547              

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Language(s): eng - English
 Dates: 2008
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 401321
 Degree: -

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Title: Neurology
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 70 (13 Pt 2) Sequence Number: - Start / End Page: 1155 - 1156 Identifier: -