Functional and clinical characterization of a mutation in KCNJ2 associated with Andersen-Tawil syndrome.
Lu CW, Lin JH, Rajawat YS, Jerng H, Rami TG, Sanchez X, DeFreitas G, Carabello B, DeMayo F, Kearney DL, Miller G, Li H, Pfaffinger PJ, Bowles NE, Khoury DS, Towbin JA.
Lu CW, et al. Among authors: rajawat ys.
J Med Genet. 2006 Aug;43(8):653-9. doi: 10.1136/jmg.2006.040816. Epub 2006 Mar 29.
J Med Genet. 2006.
PMID: 16571646
Free PMC article.