Barely Significant
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A CNGB1 frameshift mutation in Papillon and Phalène dogs with progressive retinal atrophy.

PLoS One · 2013 · PMC3756049 · PMID 24015210

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highly significantno p-value reported
These results indicate a highly significant association between the mutation and disease (P Fisher = 1.4×10 −8 ) when comparing genotyped homozygous affected dogs (n = 6) and dogs free of PRA using Fisher’s exact test.

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