• 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.