Figure 5From: Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutationLocation of the canine 8 bp SPTBN2 mutation in the β-III spectrin protein. Protein domains: ABD, actin binding domain. 4.1, protein 4.1 binding domain. ANK, ankyrin binding domain. PH, pleckstrin homology domain. MAD1; MAD2, membrane associated domains. Adapted from Bauer et al.[25].Back to article page