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McTague, Amy and Nair, Umesh and Malhotra, Sony and Meyer, Esther and Trump, Natalie and Gazina, Elena V. and Papandreou, Apostolos and Ngho, Adeline and Ackermann, Sally and Ambegaonkar, Gautam and Appleton, Richard and Desurkar, Archana and Eltze, Christin and Kneen, Rachel and Kumar, Ajith V. and Lascelles, Karine and Montgomery, Tara and Ramesh, Venkateswaran and Samanta, Rajib and Scott, Richard H. and Tan, Jeen and Whitehouse, William and Poduri, Annapurna and Scheffer, Ingrid E. and Chong, W.K. “Kling ” and Cross, J.Helen and Topf, Maya and Petrou, Steven and Kurian, Manju A. (2018) Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy. Neurology, 90 . e1-e12. ISSN 1526-632X

McTague, Amy and Nair, Umesh and Malhotra, Shalini and Meyer, Esther and Trump, Natalie and Gazina, Elena V. and Papandreou, Apostolos and Ngho, Adeline and Ackermann, Sally and Ambegaonkar, Gautam and Appleton, Richard and Desurkar, Archana and Eltze, Christin and Kneen, Rachel and Kumar, Ajith V. and Lascelles, Karine and Montgomery, Tara and Ramesh, Venkateswaran and Samanta, Rajib and Scott, Richard H. and Tan, Jeen and Whitehouse, William P. and Poduri, Annapurna and Scheffer, Ingrid E. and Chong, W.K. “Kling ” and Cross, J.Helen and Topf, M and Petrou, S and Kurian, Manju A. (2018) Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy. Neurology, 90 (1). 055. ISSN 1526-632X

Symonds, Joseph D. and Joss, Shelagh and Metcalfe, Kay A. and Somarathi, Suresh and Cruden, Jamie and Devlin, Anita M. and Donaldson, Alan and DiDonato, Nataliya and Fitzpatrick, David and Kaiser, Frank J. and Lampe, Anne K. and Lees, Melissa M. and McLellan, Ailsa and Montgomery, Tara and Mundada, Vivek and Nairn, Lesley and Sarkar, Ajoy and Schallner, Jens and Pozojevic, J.elena and Parenti, Ilaria and Tan, Jeen and Turnpenny, Peter and Whitehouse, William P. and Zuberi, Sameer M. (2017) Heterozygous truncation mutations of the SMC1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new cases. Epilepsia, 58 (4). pp. 565-575. ISSN 0013-9580