Three novel genomic loci – distinct stretches of genetic material on chromosomes – linked to Fuchs endothelial corneal dystrophy (FECD), which often clusters in families and is roughly 39 percent heritable, have been identified by researchers. Using genome-wide association data, they deepen understanding of Fuchs endothelial corneal dystrophy, the most common cause for corneal transplants.
from Top Health News – ScienceDaily http://bit.ly/2old73B
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