QTL analysis of modifiers for pigmentary disorder in rats carrying Ednrb sl mutations.

Sci Rep · 2016 · PMC4726237 · PMID 26796131

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highly significantno p-value reported

A highly significant QTL, constituting 26% of the total pigmentation phenotype variance, was identified in a region around D7Got23 on chromosome (Chr) 7.

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