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Oxford University Press

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Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families

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Fine mapping of the α-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees

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Human Molecular Genetics, Vol. 12, Iss. 23, 2003-12 ,pp. : 3133-3143

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Potential late-onset Alzheimer's disease-associated mutations in the ADAM10 gene attenuate -secretase activity

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Human Molecular Genetics, Vol. 18, Iss. 20, 2009-10 ,pp. : 3987-3996

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A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction

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