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Issue Date
Title
Author(s)
2014
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations
Scheffer, I.
;
Heron, S.
;
Regan, B.
;
Mandelstam, S.
;
Crompton, D.
;
Hodgson, B.
;
Licchetta, L.
;
Provini, F.
;
Bisulli, F.
;
Vadlamudi, L.
;
Gecz, J.
;
Connelly, A.
;
Tinuper, P.
;
Ricos, M.
;
Berkovic, S.
;
Dibbens, L.
2010
Genetics of the epilepsies: Genetic twists in the channels and other tales
Scheffer, I.
;
Zhang, Y.
;
Gecz, J.
;
Dibbens, L.
2010
Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families
Hynes, K.
;
Tarpey, P.
;
Dibbens, L.
;
Bayly, M.
;
Berkovic, S.
;
Smith, R.
;
Al Raisi, Z.
;
Turner, S.
;
Brown, N.
;
Desai, T.
;
Haan, E.
;
Turner, G.
;
Christodoulou, J.
;
Leonard, H.
;
Gill, D.
;
Stratton, M.
;
Gecz, J.
;
Scheffer, I.
Discover
Author
2
Berkovic, S.
1
Al Raisi, Z.
1
Bayly, M.
1
Bisulli, F.
1
Brown, N.
1
Christodoulou, J.
1
Connelly, A.
1
Crompton, D.
1
Desai, T.
1
Gill, D.
.
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Subject
1
Amino Acid Sequence
1
Base Sequence
1
Cadherins
1
Child Development Disorders, Perv...
1
Electroencephalography
1
Epilepsies, Partial
1
Family
1
Family Characteristics
1
GTPase-Activating Proteins
1
Magnetic Resonance Imaging
.
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Date issued
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2014
2
2010