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Non-syndromic Hearing Impairment (DFNB1 locus)

European Journal of Human Genetics (2013) 21, 1325–1329

Output from a Best Practice meeting organised by EMQN in Nijmegen, Netherlands in October 2009 to discuss and formulate consensus-based Best Practice Guide- lines for the molecular diagnosis of deafness caused by mutations at the DFNB1 locus.

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