Variant detection and runs of homozygosity in next generation sequencing data elucidate the genetic background of Lundehund syndrome.

Genome-wide association analysis for LS in 17 LS-affected and 8 LS-unaffected Lundehund showed a highly significant peak on CFA 34 at 26,384,304-27,498,705 bp (CanFam 2.0) corresponding to 23,373,982-24,488,983 bp in CanFam 3.1 assembly (Fig. 3 ) in the region of fibroblast growth factor 12 ( FGF12 ; ENSCAFG00000031187) and mab-21 domain containing 2 ( MB21D2 ; ENSCAFG00000014075).

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