Learn more:

•      Neonatal ataxia in Coton de Tulear (BNAt)

•      Primary hyperoxaluria type I (PH I)

•      Progressive retinal atrophy (PRA-PRCD)

•      Von Willebrand disease type I (VWD1)

•      Chondrodysplasia, chondrodystrophy and degeneration of intervertebral discs (CDPA/CDDY – IVDD)

DNA test sample: EDTA whole blood (1.0 ml) or buccal swabs. Detailed information about sampling can be found here.