Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice-Reference-Cited by-同舟云学术

Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice

Published:2000-12-15 Issue:12 Volume:106 Page:1447-1455
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Lee Maxwell P.,Ravenel Jason D.,Hu Ren-Ju,Lustig Lawrence R.,Tomaselli Gordon,Berger Ronald D.,Brandenburg Sheri A.,Litzi Tracy J.,Bunton Tracie E.,Limb Charles,Francis Howard,Gorelikow Melissa,Gu Hua,Washington Kay,Argani Pedram,Goldenring James R.,Coffey Robert J.,Feinberg Andrew P.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference38 articles.

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

2. KCNE1 mutations cause Jervell and Lange-Nielsen syndrome

3. Mutations in the hminK gene cause long QT syndrome and suppress lKs function

4. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

5. Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements

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