A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family
10.1055/s-2000-15290
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sg-nus-scholar.10635-1133292024-11-11T09:44:31Z A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family Lee, W.L. Biervert, C. Hallmann, K. Tay, A. Dean, J.C.S. Steinlein, O.K. PAEDIATRICS Epilepsy Gene mutation Potassium channel 10.1055/s-2000-15290 Neuropediatrics 31 1 9-12 NRPDD 2014-12-01T06:53:16Z 2014-12-01T06:53:16Z 2000-02 Article Lee, W.L., Biervert, C., Hallmann, K., Tay, A., Dean, J.C.S., Steinlein, O.K. (2000-02). A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family. Neuropediatrics 31 (1) : 9-12. ScholarBank@NUS Repository. https://doi.org/10.1055/s-2000-15290 0174304X http://scholarbank.nus.edu.sg/handle/10635/113329 000086664500003 Scopus |
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Epilepsy Gene mutation Potassium channel |
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Epilepsy Gene mutation Potassium channel Lee, W.L. Biervert, C. Hallmann, K. Tay, A. Dean, J.C.S. Steinlein, O.K. A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family |
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10.1055/s-2000-15290 |
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PAEDIATRICS |
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PAEDIATRICS Lee, W.L. Biervert, C. Hallmann, K. Tay, A. Dean, J.C.S. Steinlein, O.K. |
format |
Article |
author |
Lee, W.L. Biervert, C. Hallmann, K. Tay, A. Dean, J.C.S. Steinlein, O.K. |
author_sort |
Lee, W.L. |
title |
A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family |
title_short |
A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family |
title_full |
A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family |
title_fullStr |
A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family |
title_full_unstemmed |
A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family |
title_sort |
kcnq2 splice site mutation causing benign neonatal convulsions in a scottish family |
publishDate |
2014 |
url |
http://scholarbank.nus.edu.sg/handle/10635/113329 |
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1821189339295514624 |