Authors:
Schwartz, PJ
Priori, SG
Spazzolini, C
Moss, AJ
Vincent, GM
Napolitano, C
Denjoy, I
Guicheney, P
Breithardt, G
Keating, MT
Towbin, JA
Beggs, AH
Brink, P
Wilde, AAM
Toivonen, L
Zareba, W
Robinson, JL
Timothy, KW
Corfield, V
Wattanasirichaigoon, D
Corbett, C
Haverkamp, W
Schulze-Bahr, E
Lehmann, MH
Schwartz, K
Coumel, P
Bloise, R
Citation: Pj. Schwartz et al., Genotype-phenotype correlation in the long-QT syndrome - Gene-specific triggers for life-threatening arrhythmias, CIRCULATION, 103(1), 2001, pp. 89-95
Authors:
Nowak, KJ
Wattanasirichaigoon, D
Goebel, HH
Wilce, M
Pelin, K
Donner, K
Jacob, RL
Hubner, C
Oexle, K
Anderson, JR
Verity, CM
North, KN
Iannaccone, ST
Muller, CR
Nurnberg, P
Muntoni, F
Sewry, C
Hughes, I
Sutphen, R
Lacson, AG
Swoboda, KJ
Vigneron, J
Wallgren-Pettersson, C
Beggs, AH
Laing, NG
Citation: Kj. Nowak et al., Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy, NAT GENET, 23(2), 1999, pp. 208-212
Authors:
North, KN
Yang, N
Wattanasirichaigoon, D
Mills, M
Easteal, S
Beggs, AH
Citation: Kn. North et al., A common nonsense mutation results in alpha-actinin-3 deficiency in the general population, NAT GENET, 21(4), 1999, pp. 353-354
Authors:
Wattanasirichaigoon, D
Vesely, MR
Duggal, P
Levine, JC
Blume, ED
Wolff, GS
Edwards, SB
Beggs, AH
Citation: D. Wattanasirichaigoon et al., Sodium channel abnormalities are infrequent in patients with long QT syndrome: Identification of two novel SCN5A mutations, AM J MED G, 86(5), 1999, pp. 470-476
Authors:
Pelin, K
Hilpela, P
Donner, K
Sewry, C
Akkari, PA
Wilton, SD
Wattanasirichaigoon, D
Bang, ML
Centner, T
Hanefeld, F
Odent, S
Fardeau, M
Urtizberea, JA
Muntoni, F
Dubowitz, V
Beggs, AH
Laing, NG
Labeit, S
de la Chapelle, A
Wallgren-Pettersson, C
Citation: K. Pelin et al., Mutations in the nebulin gene associated with autosomal recessive nemalinemyopathy, P NAS US, 96(5), 1999, pp. 2305-2310