Schuele, R;
Timmann, D;
Erasmus, CE;
Reichbauer, J;
Wayand, M;
van de Warrenburg, B;
Schoels, L;
... Synofzik, M; + view all
(2021)
Solving unsolved rare neurological diseases-a Solve-RD viewpoint.
European Journal of Human Genetics
, 29
(9)
pp. 1332-1336.
10.1038/s41431-021-00901-1.
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| Type: | Article |
|---|---|
| Title: | Solving unsolved rare neurological diseases-a Solve-RD viewpoint |
| Open access status: | An open access version is available from UCL Discovery |
| DOI: | 10.1038/s41431-021-00901-1 |
| Publisher version: | https://doi.org/10.1038/s41431-021-00901-1 |
| Language: | English |
| Additional information: | © The Author(s) 2021. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
| Keywords: | Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, Genetics & Heredity |
| UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Department of Neuromuscular Diseases |
| URI: | https://discovery-pp.ucl.ac.uk/id/eprint/10138616 |
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