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. Author manuscript; available in PMC: 2018 Feb 1.
Published in final edited form as: Neuromuscul Disord. 2016 Nov 24;27(2):136–140. doi: 10.1016/j.nmd.2016.11.014

Fig. 1.

Fig. 1

Percentage of identified genetic CMS mutations in the study by kinships. Mutations in RAPSN were the most prevalent among kinships in Israel (13 kinships, 37%), followed by mutations in COLQ (11 kinships, 31%) and CHRNE (7 kinships, 20%).