Authors:
Ficker, E
Thomas, D
Viswanathan, PC
Dennis, AT
Priori, SG
Napolitano, C
Memmi, M
Wible, BA
Kaufman, ES
Iyengar, S
Schwartz, PJ
Rudy, Y
Brown, AM
Citation: E. Ficker et al., Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome, AM J P-HEAR, 279(4), 2000, pp. H1748-H1756
Authors:
Ficker, E
Dennis, AT
Obejero-Paz, CA
Castaldo, P
Taglialatela, M
Brown, AM
Citation: E. Ficker et al., Retention in the endoplasmic reticulum as a mechanism of dominant-negativecurrent suppression in human long QT syndrome, J MOL CEL C, 32(12), 2000, pp. 2327-2337
Authors:
Bianchi, L
Shen, ZJ
Dennis, AT
Priori, SG
Napolitano, C
Ronchetti, E
Bryskin, R
Schwartz, PJ
Brown, AM
Citation: L. Bianchi et al., Cellular dysfunction of LQT5-minK mutants: abnormalities of I-Ks, I-Kr andtrafficking in long QT syndrome, HUM MOL GEN, 8(8), 1999, pp. 1499-1507
Authors:
Bianchi, L
Shen, ZJ
Dennis, AT
Priori, SG
Napolitano, C
Ronchetti, E
Bryskin, R
Schwartz, PJ
Brown, AM
Citation: L. Bianchi et al., Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome (vol 8, 1499, 1999), HUM MOL GEN, 8(12), 1999, pp. 2335-2335