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.

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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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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-21A5-2 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-21A6-F

Genre: Journal Article

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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: Date issued: 2008

Publication Status: Issued

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Identifiers: eDoc: 401321

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Title: Neurology

Source Genre: Journal

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Pages: - Volume / Issue: 70 (13 Pt 2) Sequence Number: - Start / End Page: 1155 - 1156 Identifier: -