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Michael S. Hildebrand
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Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1.
?
TBD
article published in 2008
Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children.
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TBD
scientific article
A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing loss
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TBD
scientific article published in December 2010