Barely Significant
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Mutations in the gene DNAJC5 cause autosomal dominant Kufs disease in a proportion of cases: study of the Parry family and 8 other families.

PLoS One · 2012 · PMC3250487 · PMID 22235333

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highly significantno p-value reported
Discussion We have performed exome sequencing on a large pedigree with ADKD and identified two highly significant changes in two neighboring genes on chromosome 20, which segregated with the phenotype.

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