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Publication : Ankyrin-B syndrome: enhanced cardiac function balanced by risk of cardiac death and premature senescence.

First Author  Mohler PJ Year  2007
Journal  PLoS One Volume  2
Issue  10 Pages  e1051
PubMed ID  17940615 Mgi Jnum  J:130060
Mgi Id  MGI:3770697 Doi  10.1371/journal.pone.0001051
Citation  Mohler PJ, et al. (2007) Ankyrin-B syndrome: enhanced cardiac function balanced by risk of cardiac death and premature senescence. PLoS One 2(10):e1051
abstractText  Here we report the unexpected finding that specific human ANK2 variants represent a new example of balanced human variants. The prevalence of certain ANK2 (encodes ankyrin-B) variants range from 2 percent of European individuals to 8 percent in individuals from West Africa. Ankyrin-B variants associated with severe human arrhythmia phenotypes (eg E1425G, V1516D, R1788W) were rare in the general population. Variants associated with less severe clinical and in vitro phenotypes were unexpectedly common. Studies with the ankyrin-B(+/-) mouse reveal both benefits of enhanced cardiac contractility, as well as costs in earlier senescence and reduced lifespan. Together these findings suggest a constellation of traits that we term 'ankyrin-B syndrome', which may contribute to both aging-related disorders and enhanced cardiac function.
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