Novel mutations consolidateKCTD7as a progressive myoclonus epilepsy gene
- Kousi, Maria
- Anttila, Verneri
- Schulz, Angela
- Calafato, Stella
- Jakkula, Eveliina
- Riesch, Erik
- Myllykangas, Liisa
- Kalimo, Hannu
- Topçu, Meral
- Gökben, Sarenur
- Alehan, Fusun
- Lemke, Johannes R
- Alber, Michael
- Palotie, Aarno
- Kopra, Outi
- Lehesjoki, Anna-Elina
- 2012-6-12
Published in:
- Journal of Medical Genetics. - BMJ. - 2012, vol. 49, no. 6, p. 391-399
- Language
-
- English
- Open access status
- green
- Identifiers
-
- DOI 10.1136/jmedgenet-2012-100859
- ISSN 0022-2593
- Persistent URL
- https://sonar.ch/global/documents/185967
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