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U-M researchers identify gene mutation that causes rare form of deafness
Date:7/12/2010

h. Rather than relying purely on genetic inheritance information, they combined this information with biological function regarding gene activity.

"The approach we used here of combining genetic inheritance with functional information can be applied to identify the culprit genes in many other rare genetic diseases that have so far been impossible to nail down," says Burmeister, professor of Psychiatry and Human Genetics.

"We can now say we have a tool by combining several genomic approaches to find these genes."


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Contact: Mary F. Masson
mfmasson@umich.edu
734-764-2220
University of Michigan Health System
Source:Eurekalert

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