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Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?
Kokotas, Haris, Grigoriadou, Maria, Korres, George S, Ferekidou, Elisabeth, Giannoulia-Karantana, Aglaia, Kandiloros, Dimitrios, Korres, Stavros, Petersen, Michael BVolume:
55
Language:
english
Journal:
Journal of Human Genetics
DOI:
10.1038/jhg.2010.23
Date:
May, 2010
File:
PDF, 240 KB
english, 2010