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Journal Article
Hicks, D., Farsani, G. Torabi, Laval, S., Collins, J., Martoni, E., Shah, A., Zou, Y., Koch, M., Bonnemann, C., Lochmuller, H., Bushby, K., Roberts, M. and Straub, V. (2013). Collagen XII as a new disease gene for Bethlem-like myopathy. Neuromusc. Disord., 23 (9-10). S. 739 - 740. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 0960-8966
Turner, C., Brice, A., Bushby, K., Riess, O., Hanna, M., van Ommen, G., Muntoni, F., Klockgether, T., Wirth, B., Lochmueller, H., Timmerman, V., Schoells, L., Straub, V. and Tabrizi, S. (2015). NeurOmics: EU-funded-omics research for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases. Neuromusc. Disord., 25. S. S298 - 2. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364
Turner, C., Bushby, K., Johnston, L., Lochmueller, H., Riess, O., Wirth, B., Straub, V., Thompson, R. and van Ommen, G. (2015). Collaboration in NeurOmics: Enabling effective data-sharing and maximising impact in neuromuscular disease. Neuromusc. Disord., 25. S. S298 - 1. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364
Zou, Y., Zwolanek, D., Hu, Y., Schreiber, G., Brockmann, K., Izu, Y., Tian, Z., Devoto, M., Gandhy, S., Meier, M., Stetefeld, J., Hicks, D., Straub, V., Voermans, N., Birk, D. E., Barton, E. R., Koch, M. and Boennemann, C. G. (2013). Collagen type XII: A new congenital matrix and muscle disease. Neuromusc. Disord., 23 (9-10). S. 739 - 741. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 0960-8966