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Oxford University Press

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Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quaking viable mutant mouse

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Carrier frequencies of eleven mutations in eight genes associated with primary ciliary dyskinesia in the Ashkenazi Jewish population

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John Wiley & Sons Inc

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Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

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An axonemal dynein at the locus: implications for haplotype-specific male sterility and the evolution of species barriers

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