Fig. 1
From: A novel recessive mutation affecting DNAJB6a causes myofibrillar myopathy
Schematic representation of the DNAJB6 gene exons, DNAJB6 protein isoforms and the mutation. a Sequence comparison of the wildtype DNAJB6a, DNAJB6b and mutant DNAJB6a in human. b Sequence comparison of the wildtype DNAJB6a, DNAJB6b and mutant DNAJB6a in mouse. Note that the alternatively spliced C-terminal part of the “a” or “b” region is identified as the marker of the DNAJB6 isoform