A new molecular process that causes a genetic form of non-syndromic deafness has been identified by scientists. A multi-national research team led by scientists at Cincinnati Children's Hospital Medical Center report their findings in a study posted online Aug. 27 by the iJournal of Clinical Investigation/i. The research opens the door to finding possible treatments for the condition (called DFNB49 non-syndromic hearing loss) and points to possible cellular ...You have just read an article categorized health
titled Molecular Process Behind Form of Non-syndromic Deafness Discovered.
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editor - Tuesday, August 27, 2013
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