Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients. за авторством Petrie, K, Lee, W, Bullock, A, Pointon, J, Smith, R, Russell, R, Brown, M, Wordsworth, B, Triffitt, J

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Crystal structures of human HMG-CoA synthase isoforms provide insights into inherited ketogenesis disorders and inhibitor design. за авторством Shafqat, N, Turnbull, A, Zschocke, J, Oppermann, U, Yue, W

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Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-CoA mutase and insight into their complex formation за авторством Froese, D, Kochan, G, Muniz, J, Wu, X, Gileadi, C, Ugochukwu, E, Krysztofinska, E, Gravel, R, Oppermann, U, Yue, W

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