Skip to main content
. 2016 Aug 24;311(5):C749–C757. doi: 10.1152/ajpcell.00134.2016

Fig. 1.

Fig. 1.

Skeletal disease-associated mutations in RyR1. Amino acid sequences of three domains are shown. Underlines indicate EF-hand motifs. Bold letters denote MH, CCD, or CNM-linked mutation sites (https://cardiodb.org/Paralogue_Annotation/). Mutation sites characterized in this study are highlighted in gray, and mutations are shown in italic below the sequence.