2010•Journal of Human GeneticsRequires access

Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?

Haris Kokotas, Maria Grigoriadou, George Korres, Elisabeth Ferekidou, Aglaia Giannoulia‐Karantana, Dimitrios Kandiloros, Stavros Korres, Michael B. Petersen

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Key concepts: Penetrance, Mitochondrial DNA, Hearing loss, Genetics, Phenotype, Biology, Mutation, Gene

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Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness? — Research Paper | ScholarLens