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Issue Date
Title
Author(s)
2021
Association of SLC32A1 missense variants with genetic epilepsy with febrile seizures plus
Heron, S.E.
;
Regan, B.M.
;
Harris, R.V.
;
Gardner, A.E.
;
Coleman, M.J.
;
Bennett, M.F.
;
Grinton, B.E.
;
Helbig, K.L.
;
Sperling, M.R.
;
Haut, S.
;
Geller, E.B.
;
Widdess-Walsh, P.
;
Pelekanos, J.T.
;
Bahlo, M.
;
Petrovski, S.
;
Heinzen, E.L.
;
Hildebrand, M.S.
;
Corbett, M.A.
;
Scheffer, I.E.
;
Gecz, J.
;
et al.
2020
Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian families
Bennett, M.F.
;
Oliver, K.L.
;
Regan, B.M.
;
Bellows, S.T.
;
Schneider, A.L.
;
Rafehi, H.
;
Sikta, N.
;
Crompton, D.E.
;
Coleman, M.
;
Hildebrand, M.S.
;
Corbett, M.A.
;
Kroes, T.
;
Gecz, J.
;
Scheffer, I.E.
;
Berkovic, S.F.
;
Bahlo, M.
2020
SCN1A Variants in vaccine-related febrile seizures: a prospective study
Damiano, J.A.
;
Deng, L.
;
Li, W.
;
Burgess, R.
;
Schneider, A.L.
;
Crawford, N.W.
;
Buttery, J.
;
Gold, M.
;
Richmond, P.
;
Macartney, K.K.
;
Hildebrand, M.S.
;
Scheffer, I.E.
;
Wood, N.
;
Berkovic, S.F.
Discover
Author
3
Scheffer, I.E.
2
Bahlo, M.
2
Bennett, M.F.
2
Berkovic, S.F.
2
Corbett, M.A.
2
Gecz, J.
2
Regan, B.M.
2
Schneider, A.L.
1
Bellows, S.T.
1
Burgess, R.
.
next >
Subject
3
Humans
3
Male
2
Mutation
2
Pedigree
2
Seizures, Febrile
1
Case-Control Studies
1
Child, Preschool
1
Epilepsies, Myoclonic
1
Epilepsy, Generalized
1
Founder Effect
.
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Date issued
1
2021
2
2020