Loss of glycosylation associated with the T183A mutation in human prion disease. | Acta Neuropathol;108(6): 476-84, 2004 Dec. | MEDLINE

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Loss of glycosylation associated with the T183A mutation in human prion disease.

Grasbon-Frodl, E; Lorenz, Holger; Mann, U; Nitsch, R M; Windl, Otto; Kretzschmar, H A.

Affiliation

Grasbon-Frodl E; Center for Neuropathology and Prion Research, University of Munich, Feodor-Lynen-Str. 23, 81377 München, Germany.

Acta Neuropathol ; 108(6): 476-84, 2004 Dec.

Article in En | MEDLINE | ID: mdl-15558291

Subject(s)

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Collection: 01-internacional Database: MEDLINE Main subject: Glycosylation / Brain / Prions / Creutzfeldt-Jakob Syndrome / Prion Diseases Type of study: Prognostic_studies / Risk_factors_studies Limits: Adult / Humans / Male Language: En Journal: Acta Neuropathol Year: 2004 Document type: Article Affiliation country:

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Collection: 01-internacional Database: MEDLINE Main subject: Glycosylation / Brain / Prions / Creutzfeldt-Jakob Syndrome / Prion Diseases Type of study: Prognostic_studies / Risk_factors_studies Limits: Adult / Humans / Male Language: En Journal: Acta Neuropathol Year: 2004 Document type: Article Affiliation country: