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A missense mutation in the KCTD17 gene causes autosomal dominant myoclonus-dystonia
- Authors :
- Mencacci, N. E.
Rubio-Augusti, I.
Zdebik, A.
Asmus, F.
Ludtmann, M.
Hauser, A. K.
Plagnol, V.
Pittman, A.
Bandres-Ciga, S.
Soutar, M.
Peall, K.
Morris, H.
Trabzuni, D.
Ryten, M.
Tekman, M.
Stanescu, H.
Kleta, R.
Carecchio, M.
Nardocci, N.
Barbara Garavaglia
Lohmann, E.
Weissbach, A.
Klein, C.
Hardy, J.
Abramov, A. Y.
Foltynie, T.
Gasser, T.
Bhatia, K. P.
Wood, N. W.
- Source :
- ResearcherID, Publons, Web of Science
Details
- Database :
- OpenAIRE
- Journal :
- ResearcherID, Publons, Web of Science
- Accession number :
- edsair.dedup.wf.001..0ff1a2cb7383f1511d5a56b67f133bf8