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Selected Publication:

Claeys, K; Ivanova, N; Deconinck, T; Litvinenko, I; Jordanova, A; Loefgren, A; Nelis, E; Mercelis, R; Auer-Grumbach, M; Priller, J; Ceulemans, B; Sereda, M; Kremensky, I; Mitev, V; De Jonghe, P.
SPG3A mutations are associated with pure and complex forms of Hereditary Spastic Paraplegia
NEUROMUSCULAR DISORD. 16: S63-S63. [Poster]
Web of Science

Authors Med Uni Graz:: Auer-Grumbach Michaela
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