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GORMAN, KM, MEYER, E, GROZEVA, D, SPINELLI, E, MCTAGUE, A, SANCHIS-JUAN, A, CARSS, KJ, BRYANT, E, REICH, A, SCHNEIDER, AL, PRESSLER, RM, SIMPSON, MA, DEBELLE, GD, WASSMER, E, MORTON, J, SIECIECHOWICZ, D, JAN-KAMSTEEG, E, PACIORKOWSKI, AR, KING, MD, CROSS, JH, PODURI, A, MEFFORD, HC, SCHEFFER, IE, HAACK, TB, MCCULLAGH, G, MCRAE, JF, CLAYTON, S, FITZGERALD, TW, KAPLANIS, J, PRIGMORE, E, RAJAN, D, SIFRIM, A, AITKEN, S, AKAWI, N, ALVI, M, AMBRIDGE, K, BARRETT, DM, BAYZETINOVA, T, JONES, P, JONES, WD, KING, D, KRISHNAPPA, N, MASON, LE, SINGH, T, TIVEY, AR, AHMED, M, ANJUM, U, ARCHER, H, ARMSTRONG, R, AWADA, J, BALASUBRAMANIAN, M, BANKA, S, BARALLE, D, BARNICOAT, A, BATSTONE, P, BATY, D, BENNETT, C, BERG, J, BERNHARD, B, BEVAN, AP, BITNER-GLINDZICZ, M, BLAIR, E, BLYTH, M, BOHANNA, D, BOURDON, L, BOURN, D, BRADLEY, L, BRADY, A, BRENT, S, BREWER, C, BRUNSTROM, K, BUNYAN, DJ, BURN, J, CANHAM, N, CASTLE, B, CHANDLER, K, CHATZIMICHALI, E, CILLIERS, D, CLARKE, A, CLASPER, S, CLAYTON-SMITH, J, CLOWES, V, COATES, A, COLE, T, COLGIU, I, COLLINS, A, COLLINSON, MN, CONNELL, F, COOPER, N, COX, H, CRESSWELL, L, CROSS, G, CROW, Y, D'ALESSANDRO, M, DABIR, T, DAVIDSON, R, DAVIES, S, DE VRIES, D, DEAN, J, DESHPANDE, C and CROOKS, Lucy (2019). Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia. American Journal of Human Genetics, 104 (5), 948-956. [Article]