-
1
-
-
0035956488
-
Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation
-
Abou-Khalil B, Ge Q, Desai R, Ryther R, Bazyk A, Bailey R, Haines JL, Sutcliffe JS, George Jr AL (2001) Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation. Neurology 57:2265-2272.
-
(2001)
Neurology
, vol.57
, pp. 2265-2272
-
-
Abou-Khalil, B.1
Ge, Q.2
Desai, R.3
Ryther, R.4
Bazyk, A.5
Bailey, R.6
Haines, J.L.7
Sutcliffe, J.S.8
George Jr., A.L.9
-
2
-
-
0034671216
-
A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro
-
Alekov A, Rahman MM, Mitrovic N, Lehmann-Horn F, Lerche H (2000) A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro. J Physiol (Lond) 529:533-539.
-
(2000)
J Physiol (Lond)
, vol.529
, pp. 533-539
-
-
Alekov, A.1
Rahman, M.M.2
Mitrovic, N.3
Lehmann-Horn, F.4
Lerche, H.5
-
3
-
-
0034954467
-
Enhanced inactivation and acceleration of activation of the sodium channel associated with epilepsy in man
-
Alekov AK, Rahman MM, Mitrovic N, Lehmann-Horn F, Lerche H (2001) Enhanced inactivation and acceleration of activation of the sodium channel associated with epilepsy in man. Eur J Neurosci 13:2171-2176.
-
(2001)
Eur J Neurosci
, vol.13
, pp. 2171-2176
-
-
Alekov, A.K.1
Rahman, M.M.2
Mitrovic, N.3
Lehmann-Horn, F.4
Lerche, H.5
-
4
-
-
0035030766
-
First genetic evidence of GABA(A) receptor dysfunction in epilepsy: A mutation in the gamma2-subunit gene
-
Baulac S, Huberfeld G, Gourfinkel-An I, Mitropoulou G, Beranger A, Prud'homme JF, Baulac M, Brice A, Bruzzone R, LeGuern E (2001) First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene. Nat Genet 28:46-48.
-
(2001)
Nat Genet
, vol.28
, pp. 46-48
-
-
Baulac, S.1
Huberfeld, G.2
Gourfinkel-An, I.3
Mitropoulou, G.4
Beranger, A.5
Prud'Homme, J.F.6
Baulac, M.7
Brice, A.8
Bruzzone, R.9
LeGuern, E.10
-
5
-
-
0036663012
-
Two different mechanisms of disinhibition produced by GABAA receptor mutations linked to epilepsy in humans
-
Bianchi MT, Song L, Zhang H, Macdonald RL (2002) Two different mechanisms of disinhibition produced by GABAA receptor mutations linked to epilepsy in humans. J Neurosci 22:5321-5327.
-
(2002)
J Neurosci
, vol.22
, pp. 5321-5327
-
-
Bianchi, M.T.1
Song, L.2
Zhang, H.3
Macdonald, R.L.4
-
6
-
-
0034987073
-
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy
-
Claes L, Del Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P (2001) De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. Am J Hum Genet 68:1327-1332.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1327-1332
-
-
Claes, L.1
Del Favero, J.2
Ceulemans, B.3
Lagae, L.4
Van Broeckhoven, C.5
De Jonghe, P.6
-
7
-
-
0038240713
-
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy
-
Claes L, Ceulemans B, Audenaert D, Smets K, Lofgren A, Del Favero J, Ala-Mello S, Basel-Vanagaite L, Plecko B, Raskin S, Thiry P, Wolf NI, Van Broeckhoven C, De Jonghe P (2003) De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy. Hum Mutat 21:615-621.
-
(2003)
Hum Mutat
, vol.21
, pp. 615-621
-
-
Claes, L.1
Ceulemans, B.2
Audenaert, D.3
Smets, K.4
Lofgren, A.5
Del Favero, J.6
Ala-Mello, S.7
Basel-Vanagaite, L.8
Plecko, B.9
Raskin, S.10
Thiry, P.11
Wolf, N.I.12
Van Broeckhoven, C.13
De Jonghe, P.14
-
8
-
-
12244289247
-
Functional characterization of the D188V mutation in neuronal voltage-gated sodium channel causing generalized epilepsy with febrile seizures plus (GEFS)
-
Cossette P, Loukas A, Lafreniere RG, Rochefort D, Harvey-Girard E, Ragsdale DS, Dunn RJ, Rouleau GA (2003) Functional characterization of the D188V mutation in neuronal voltage-gated sodium channel causing generalized epilepsy with febrile seizures plus (GEFS). Epilepsy Res 53:107-117.
-
(2003)
Epilepsy Res
, vol.53
, pp. 107-117
-
-
Cossette, P.1
Loukas, A.2
Lafreniere, R.G.3
Rochefort, D.4
Harvey-Girard, E.5
Ragsdale, D.S.6
Dunn, R.J.7
Rouleau, G.A.8
-
9
-
-
0019804952
-
The benign myoclonic epilepsy of infancy (author's translation)
-
Dravet C, Bureau M (1981) The benign myoclonic epilepsy of infancy (author's translation). Rev Electroencephalogr Neurophysiol Clin 11:438-444.
-
(1981)
Rev Electroencephalogr Neurophysiol Clin
, vol.11
, pp. 438-444
-
-
Dravet, C.1
Bureau, M.2
-
10
-
-
0036115199
-
Calcium-pump inhibitors induce functional surface expression of delta F508-CFTR protein in cystic fibrosis epithelial cells
-
Egan ME, Glockner-Pagel J, Ambrose C, Cahill PA, Pappoe L, Balamuth N, Cho E, Canny S, Wagner CA, Geibel J, Caplan MJ (2002) Calcium-pump inhibitors induce functional surface expression of delta F508-CFTR protein in cystic fibrosis epithelial cells. Nat Med 8:485-492.
-
(2002)
Nat Med
, vol.8
, pp. 485-492
-
-
Egan, M.E.1
Glockner-Pagel, J.2
Ambrose, C.3
Cahill, P.A.4
Pappoe, L.5
Balamuth, N.6
Cho, E.7
Canny, S.8
Wagner, C.A.9
Geibel, J.10
Caplan, M.J.11
-
11
-
-
0034069651
-
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2
-
Escayg A, MacDonald BT, Meisler MH, Baulac S, Huberfeld G, An-Gourfinkel I, Brice A, LeGuern E, Moulard B, Chaigne D, Buresi C, Malafosse A (2000) Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2. Nat Genet 24:343-345.
-
(2000)
Nat Genet
, vol.24
, pp. 343-345
-
-
Escayg, A.1
MacDonald, B.T.2
Meisler, M.H.3
Baulac, S.4
Huberfeld, G.5
An-Gourfinkel, I.6
Brice, A.7
LeGuern, E.8
Moulard, B.9
Chaigne, D.10
Buresi, C.11
Malafosse, A.12
-
12
-
-
0035071143
-
A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus-and prevalence of variants in patients with epilepsy
-
Escayg A, Heils A, MacDonald BT, Haug K, Sander T, Meisler MH (2001) A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus-and prevalence of variants in patients with epilepsy. Am J Hum Genet 68:866-873.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 866-873
-
-
Escayg, A.1
Heils, A.2
MacDonald, B.T.3
Haug, K.4
Sander, T.5
Meisler, M.H.6
-
13
-
-
0029785795
-
A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo
-
French PJ, van Doorninck JH, Peters RH, Verbeek E, Ameen NA, Marino CR, de Jonge HR, Bijman J, Scholte BJ (1996) A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo. J Clin Invest 98:1304-1312.
-
(1996)
J Clin Invest
, vol.98
, pp. 1304-1312
-
-
French, P.J.1
Van Doorninck, J.H.2
Peters, R.H.3
Verbeek, E.4
Ameen, N.A.5
Marino, C.R.6
De Jonge, H.R.7
Bijman, J.8
Scholte, B.J.9
-
14
-
-
0344672944
-
Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures
-
Fujiwara T, Sugawara T, Mazaki-Miyazaki E, Takahashi Y, Fukushima K, Watanabe M, Hara K, Morikawa T, Yagi K, Yamakawa K, Inoue Y (2003) Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures. Brain 126:531-546.
-
(2003)
Brain
, vol.126
, pp. 531-546
-
-
Fujiwara, T.1
Sugawara, T.2
Mazaki-Miyazaki, E.3
Takahashi, Y.4
Fukushima, K.5
Watanabe, M.6
Hara, K.7
Morikawa, T.8
Yagi, K.9
Yamakawa, K.10
Inoue, Y.11
-
15
-
-
0036158906
-
Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A
-
Ito M, Nagafuji H, Okazawa H, Yamakawa K, Sugawara T, Mazaki-Miyazaki E, Hirose S, Fukuma G, Mitsudome A, Wada K, Kaneko S (2002) Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+) -channel alpha 1 subunit gene, SCN1A. Epilepsy Res 48:15-23.
-
(2002)
Epilepsy Res
, vol.48
, pp. 15-23
-
-
Ito, M.1
Nagafuji, H.2
Okazawa, H.3
Yamakawa, K.4
Sugawara, T.5
Mazaki-Miyazaki, E.6
Hirose, S.7
Fukuma, G.8
Mitsudome, A.9
Wada, K.10
Kaneko, S.11
-
16
-
-
0035863416
-
A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities
-
Kearney JA, Plummer NW, Smith MR, Kapur J, Cummins TR, Waxman SG, Goldin AL, Meisler MH (2001) A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities. Neuroscience 102:307-317.
-
(2001)
Neuroscience
, vol.102
, pp. 307-317
-
-
Kearney, J.A.1
Plummer, N.W.2
Smith, M.R.3
Kapur, J.4
Cummins, T.R.5
Waxman, S.G.6
Goldin, A.L.7
Meisler, M.H.8
-
17
-
-
0037071896
-
Molecular basis of an inherited epilepsy
-
Lossin C, Wang DW, Rhodes TH, Vanoye CG, George Jr AL (2002) Molecular basis of an inherited epilepsy. Neuron 34:877-884.
-
(2002)
Neuron
, vol.34
, pp. 877-884
-
-
Lossin, C.1
Wang, D.W.2
Rhodes, T.H.3
Vanoye, C.G.4
George Jr., A.L.5
-
19
-
-
10744226685
-
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy
-
Nabbout R, Gennaro E, Dalla BB, Dulac O, Madia F, Bertini E, Capovilla G, Chiron, C, Cristofori G, Elia M, Fontana E, Gaggero R, Granata T, Guerrini R, Loi M, La Selva L, Lispi ML, Matricardi A, Romeo A, Tzolas V, Valseriati D, Veggiotti P, Vigevano F, Vallee L, Dagna BF, Bianchi A, Zara F (2003) Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy. Neurology 60:1961-1967.
-
(2003)
Neurology
, vol.60
, pp. 1961-1967
-
-
Nabbout, R.1
Gennaro, E.2
Dalla, B.B.3
Dulac, O.4
Madia, F.5
Bertini, E.6
Capovilla, G.7
Chiron, C.8
Cristofori, G.9
Elia, M.10
Fontana, E.11
Gaggero, R.12
Granata, T.13
Guerrini, R.14
Loi, M.15
La Selva, L.16
Lispi, M.L.17
Matricardi, A.18
Romeo, A.19
Tzolas, V.20
Valseriati, D.21
Veggiotti, P.22
Vigevano, F.23
Vallee, L.24
Dagna, B.F.25
Bianchi, A.26
Zara, F.27
more..
-
20
-
-
0036304363
-
Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy
-
Ohmori I, Ouchida M, Ohtsuka Y, Oka E, Shimizu K (2002) Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy. Biochem Biophys Res Commun 295:17-23.
-
(2002)
Biochem Biophys Res Commun
, vol.295
, pp. 17-23
-
-
Ohmori, I.1
Ouchida, M.2
Ohtsuka, Y.3
Oka, E.4
Shimizu, K.5
-
21
-
-
0036133994
-
Channelopathies: Episodic disorders of the nervous system
-
Ptacek L (2002) Channelopathies: episodic disorders of the nervous system. Novartis Found Symp 241:87-104.
-
(2002)
Novartis Found Symp
, vol.241
, pp. 87-104
-
-
Ptacek, L.1
-
22
-
-
0037129911
-
Pharmacological rescue of human K(+) channel long-QT2 mutations: Human ether-a-go-go-related gene rescue without block
-
Rajamani S, Anderson CL, Anson BD, January CT (2002) Pharmacological rescue of human K(+) channel long-QT2 mutations: human ether-a-go-go-related gene rescue without block. Circulation 105:2830-2835.
-
(2002)
Circulation
, vol.105
, pp. 2830-2835
-
-
Rajamani, S.1
Anderson, C.L.2
Anson, B.D.3
January, C.T.4
-
23
-
-
0030809817
-
In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR
-
Rubenstein RC, Egan ME, Zeitlin PL (1997) In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR. J Clin Invest 100:2457-2465.
-
(1997)
J Clin Invest
, vol.100
, pp. 2457-2465
-
-
Rubenstein, R.C.1
Egan, M.E.2
Zeitlin, P.L.3
-
24
-
-
0030042386
-
Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation
-
Sato S, Ward CL, Krouse ME, Wine JJ, Kopito RR (1996) Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation. J Biol Chem 271:635-638.
-
(1996)
J Biol Chem
, vol.271
, pp. 635-638
-
-
Sato, S.1
Ward, C.L.2
Krouse, M.E.3
Wine, J.J.4
Kopito, R.R.5
-
25
-
-
0030943313
-
Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes
-
Scheffer IE, Berkovic SF (1997) Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes. Brain 120:479-490.
-
(1997)
Brain
, vol.120
, pp. 479-490
-
-
Scheffer, I.E.1
Berkovic, S.F.2
-
26
-
-
0034783413
-
Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome)
-
Scheffer IE, Wallace R, Mulley JC, Berkovic SF (2001) Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome). Brain Dev 23:732-735.
-
(2001)
Brain Dev
, vol.23
, pp. 732-735
-
-
Scheffer, I.E.1
Wallace, R.2
Mulley, J.C.3
Berkovic, S.F.4
-
27
-
-
0034850563
-
Severe myoclonic epilepsy of infancy: Extended spectrum of GEFS+?
-
Singh R, Andermann E, Whitehouse WP, Harvey AS, Keene DL, Seni MH, Crossland KM, Andermann F, Berkovic SF, Scheffer IE (2001) Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+? Epilepsia 42:837-844.
-
(2001)
Epilepsia
, vol.42
, pp. 837-844
-
-
Singh, R.1
Andermann, E.2
Whitehouse, W.P.3
Harvey, A.S.4
Keene, D.L.5
Seni, M.H.6
Crossland, K.M.7
Andermann, F.8
Berkovic, S.F.9
Scheffer, I.E.10
-
28
-
-
0035478007
-
Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2
-
Spampanato J, Escayg A, Meisler MH, Goldin AL (2001) Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2. J Neurosci 21:7481-7490.
-
(2001)
J Neurosci
, vol.21
, pp. 7481-7490
-
-
Spampanato, J.1
Escayg, A.2
Meisler, M.H.3
Goldin, A.L.4
-
29
-
-
0346106074
-
Generalized epilepsy with febrile seizures plus type 2 mutation W1204R alters voltage-dependent gating of Na(v) 1.1 sodium channels
-
Spampanato J, Escayg A, Meisler MH, Goldin AL (2003) Generalized epilepsy with febrile seizures plus type 2 mutation W1204R alters voltage-dependent gating of Na(v) 1.1 sodium channels. Neuroscience 116:37-48.
-
(2003)
Neuroscience
, vol.116
, pp. 37-48
-
-
Spampanato, J.1
Escayg, A.2
Meisler, M.H.3
Goldin, A.L.4
-
30
-
-
0035964102
-
Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures
-
Sugawara T, Mazaki-Miyazaki E, Ito M, Nagafuji H, Fukuma G, Mitsudome A, Wada K, Kaneko S, Hirose S, Yamakawa K (2001a) Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures. Neurology 57:703-705.
-
(2001)
Neurology
, vol.57
, pp. 703-705
-
-
Sugawara, T.1
Mazaki-Miyazaki, E.2
Ito, M.3
Nagafuji, H.4
Fukuma, G.5
Mitsudome, A.6
Wada, K.7
Kaneko, S.8
Hirose, S.9
Yamakawa, K.10
-
31
-
-
14344277590
-
A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction
-
Sugawara T, Tsurubuchi Y, Agarwala KL, Ito M, Fukuma G, Mazaki-Miyazaki E, Nagafuji H, Noda M, Imoto K, Wada K, Mitsudome A, Kaneko S, Montal M, Nagata K, Hirose S, Yamakawa K (2001b) A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction. Proc Natl Acad Sci USA 98:6384-6389.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 6384-6389
-
-
Sugawara, T.1
Tsurubuchi, Y.2
Agarwala, K.L.3
Ito, M.4
Fukuma, G.5
Mazaki-Miyazaki, E.6
Nagafuji, H.7
Noda, M.8
Imoto, K.9
Wada, K.10
Mitsudome, A.11
Kaneko, S.12
Montal, M.13
Nagata, K.14
Hirose, S.15
Yamakawa, K.16
-
32
-
-
0037046207
-
Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy
-
Sugawara T, Mazaki-Miyazaki E, Fukushima K, Shimomura J, Fujiwara T, Hamano S, Inoue Y, Yamakawa K (2002) Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy. Neurology 58:1122-1124.
-
(2002)
Neurology
, vol.58
, pp. 1122-1124
-
-
Sugawara, T.1
Mazaki-Miyazaki, E.2
Fukushima, K.3
Shimomura, J.4
Fujiwara, T.5
Hamano, S.6
Inoue, Y.7
Yamakawa, K.8
-
33
-
-
0036063688
-
A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine
-
Valdivia CR, Ackerman MJ, Tester DJ, Wada T, McCormack J, Ye B, Makielski JC (2002) A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine. Cardiovasc Res 55:279-289.
-
(2002)
Cardiovasc Res
, vol.55
, pp. 279-289
-
-
Valdivia, C.R.1
Ackerman, M.J.2
Tester, D.J.3
Wada, T.4
McCormack, J.5
Ye, B.6
Makielski, J.C.7
-
34
-
-
17344367657
-
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta 1 subunit gene SCN1B
-
Wallace RH, Wang DW, Singh R, Scheffer IE, George Jr AL, Phillips HA, Saar K, Reis A, Johnson EW, Sutherland GR, Berkovic SF, Mulley JC (1998) Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta 1 subunit gene SCN1B. Nat Genet 19:366-370.
-
(1998)
Nat Genet
, vol.19
, pp. 366-370
-
-
Wallace, R.H.1
Wang, D.W.2
Singh, R.3
Scheffer, I.E.4
George Jr., A.L.5
Phillips, H.A.6
Saar, K.7
Reis, A.8
Johnson, E.W.9
Sutherland, G.R.10
Berkovic, S.F.11
Mulley, J.C.12
-
35
-
-
0035033520
-
Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures
-
Wallace RH, Marini C, Petrou S, Harkin LA, Bowser DN, Panchal RG, Williams DA, Sutherland GR, Mulley JC, Scheffer IE, Berkovic SF (2001a) Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures. Nat Genet 28:49-52.
-
(2001)
Nat Genet
, vol.28
, pp. 49-52
-
-
Wallace, R.H.1
Marini, C.2
Petrou, S.3
Harkin, L.A.4
Bowser, D.N.5
Panchal, R.G.6
Williams, D.A.7
Sutherland, G.R.8
Mulley, J.C.9
Scheffer, I.E.10
Berkovic, S.F.11
-
36
-
-
0035074294
-
Neuronal sodium-channel alpha 1-subunit mutations in generalized epilepsy with febrile seizures plus
-
Wallace RH, Scheffer IE, Barnett S, Richards M, Dibbens L, Desai RR, Lerman-Sagie T, Lev D, Mazarib A, Brand N, Ben Zeev B, Goikhman I, Singh R, Kremmidiotis G, Gardner A, Sutherland GR, George Jr AL, Mulley JC, Berkovic SF (2001b) Neuronal sodium-channel alpha 1-subunit mutations in generalized epilepsy with febrile seizures plus. Am J Hum Genet 68:859-865.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 859-865
-
-
Wallace, R.H.1
Scheffer, I.E.2
Barnett, S.3
Richards, M.4
Dibbens, L.5
Desai, R.R.6
Lerman-Sagie, T.7
Lev, D.8
Mazarib, A.9
Brand, N.10
Ben Zeev, B.11
Goikhman, I.12
Singh, R.13
Kremmidiotis, G.14
Gardner, A.15
Sutherland, G.R.16
George Jr., A.L.17
Mulley, J.C.18
Berkovic, S.F.19
-
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-
-
0034686371
-
Distribution of voltage-gated sodium channel alpha-subunit and beta-subunit mRNAs in human hippocampal formation, cortex, and cerebellum
-
Whitaker WR, Clare JJ, Powell AJ, Chen YH, Faull RL, Emson PC (2000) Distribution of voltage-gated sodium channel alpha-subunit and beta-subunit mRNAs in human hippocampal formation, cortex, and cerebellum. J Comp Neurol 422:123-139.
-
(2000)
J Comp Neurol
, vol.422
, pp. 123-139
-
-
Whitaker, W.R.1
Clare, J.J.2
Powell, A.J.3
Chen, Y.H.4
Faull, R.L.5
Emson, P.C.6
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