A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family

10.1055/s-2000-15290

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Main Authors: Lee, W.L., Biervert, C., Hallmann, K., Tay, A., Dean, J.C.S., Steinlein, O.K.
Other Authors: PAEDIATRICS
Format: Article
Published: 2014
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Online Access:http://scholarbank.nus.edu.sg/handle/10635/113329
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spelling sg-nus-scholar.10635-1133292023-10-30T22:17:40Z 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
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic Epilepsy
Gene mutation
Potassium channel
spellingShingle 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
description 10.1055/s-2000-15290
author2 PAEDIATRICS
author_facet 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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