共 3 条
[1]
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
[J].
Plaster, NM
;
Tawil, R
;
Tristani-Firouzi, M
;
Canún, S
;
Bendahhou, S
;
Tsunoda, A
;
Donaldson, MR
;
Iannaccone, ST
;
Brunt, E
;
Barohn, R
;
Clark, J
;
Deymeer, F
;
George, AL
;
Fish, FA
;
Hahn, A
;
Nitu, A
;
Ozdemir, C
;
Serdaroglu, P
;
Subramony, SH
;
Wolfe, G
;
Fu, YH
;
Ptácek, LJ
.
CELL,
2001, 105 (04)
:511-519

Plaster, NM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Tawil, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Tristani-Firouzi, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Canún, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Bendahhou, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Tsunoda, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Donaldson, MR
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Iannaccone, ST
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Brunt, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Barohn, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Clark, J
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Deymeer, F
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

George, AL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Fish, FA
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Hahn, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Nitu, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Ozdemir, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Serdaroglu, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Subramony, SH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Wolfe, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Fu, YH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA

Ptácek, LJ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA
[2]
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
[J].
Tristani-Firouzi, M
;
Jensen, JL
;
Donaldson, MR
;
Sansone, V
;
Meola, G
;
Hahn, A
;
Bendahhou, S
;
Kwiecinski, H
;
Fidzianska, A
;
Plaster, N
;
Fu, YH
;
Ptacek, LJ
;
Tawil, R
.
JOURNAL OF CLINICAL INVESTIGATION,
2002, 110 (03)
:381-388

Tristani-Firouzi, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Jensen, JL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Donaldson, MR
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Sansone, V
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Meola, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Hahn, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Bendahhou, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Kwiecinski, H
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Fidzianska, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Plaster, N
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Fu, YH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Ptacek, LJ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA

Tawil, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA
[3]
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations -: Characteristic T-U-wave patterns predict the KCNJ2 genotype
[J].
Zhang, L
;
Benson, DW
;
Tristani-Firouzi, M
;
Ptacek, LJ
;
Tawil, R
;
Schwartz, PJ
;
George, AL
;
Horie, M
;
Andelfinger, G
;
Snow, GL
;
Fu, YH
;
Ackerman, MJ
;
Vincent, GM
.
CIRCULATION,
2005, 111 (21)
:2720-2726

Zhang, L
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA

Benson, DW
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA

Tristani-Firouzi, M
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA

Ptacek, LJ
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA

Tawil, R
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA

Schwartz, PJ
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA

George, AL
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA

论文数: 引用数:
h-index:
机构:

Andelfinger, G
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA

Snow, GL
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA

Fu, YH
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA

Ackerman, MJ
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA

Vincent, GM
论文数: 0 引用数: 0
h-index: 0
机构: LDS Hosp, Dept Med, Salt Lake City, UT 84103 USA