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 ...Wednesday, 28 August 2013
Molecular Process Behind Form of Non-syndromic Deafness Discovered
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 ...
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