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The disease showed an autosomal dominant inheritance with incomplete penetrance
Mutations associated with LPN1 and LPN2 represent only 1/3 of all cases of PN in Leonberger
RNF207 Gene
Regular participation in double-blind ISAG ring trials
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Hereditäre Ataxie (HA)/ Spinocerebelläre Ataxie (SCA) – Australian Shepherd Aktionen The disease showed an autosomalHereditary ataxias occur in different dog breeds with diverse molecular etiology. In Australian Shepherds the disease was identified between 4 and 19 months of age. Initial clinical signs are moderate ataxia, more obvious on the pelvic limbs, hypermetria and slight to no proprioceptive deficits on the pelvic limbs. With the disease progression clinical signs become more prominent and include inability to walk without help, severe spasticity of the
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