U89364[Secondary Source ID] - Search Results

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Year	Number of Results
1996	2
1997	2
2025	0

Page 1

Molecular basis of the long-QT syndrome associated with deafness.

Splawski I, Timothy KW, Vincent GM, Atkinson DL, Keating MT. Splawski I, et al. N Engl J Med. 1997 May 29;336(22):1562-7. doi: 10.1056/NEJM199705293362204. N Engl J Med. 1997. PMID: 9164812 Free article. No abstract available.

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.

Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, Shen J, Timothy KW, Vincent GM, de Jager T, Schwartz PJ, Toubin JA, Moss AJ, Atkinson DL, Landes GM, Connors TD, Keating MT. Wang Q, et al. Nat Genet. 1996 Jan;12(1):17-23. doi: 10.1038/ng0196-17. Nat Genet. 1996. PMID: 8528244

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.

Sanguinetti MC, Curran ME, Zou A, Shen J, Spector PS, Atkinson DL, Keating MT. Sanguinetti MC, et al. Nature. 1996 Nov 7;384(6604):80-3. doi: 10.1038/384080a0. Nature. 1996. PMID: 8900283

George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafness.

Splawski I, Timothy KW, Vincent GM, Atkinson DL, Keating MT. Splawski I, et al. Proc Assoc Am Physicians. 1997 Sep;109(5):504-11. Proc Assoc Am Physicians. 1997. PMID: 9285950

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