Kruer, MC;
Jepperson, T;
Dutta, S;
Steiner, RD;
Cottenie, E;
Sanford, L;
Merkens, M;
... Houlden, H; + view all
(2013)
Mutations in gamma adducin are associated with inherited cerebral palsy.
Ann Neurol
, 74
(6)
pp. 805-814.
10.1002/ana.23971.
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Abstract
Cerebral palsy is estimated to affect nearly 1 in 500 children, and although prenatal and perinatal contributors have been well-characterized, at least 20% of cases are believed to be inherited. Previous studies have identified mutations in the actin-capping protein KANK1 and the adaptor protein -4 complex in forms of inherited cerebral palsy, suggesting a role for components of the dynamic cytoskeleton in the genesis of the disease.
| Type: | Article |
|---|---|
| Title: | Mutations in gamma adducin are associated with inherited cerebral palsy. |
| Open access status: | An open access version is available from UCL Discovery |
| DOI: | 10.1002/ana.23971 |
| Publisher version: | http://dx.doi.org/10.1002/ana.23971 |
| Additional information: | © 2013 American Neurological Association. Full text made available to UCL Discovery by kind permission of Wiley. |
| 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.ucl.ac.uk/id/eprint/1413050 |
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