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. 2015 Oct 30;15:223. doi: 10.1186/s12883-015-0481-3

Fig. 3.

Fig. 3

Identification of the disease-causing genetic variant. a Sequence chromatograph of a fragment of the DNM2 gene showing the position of nucleotide substitution (arrow) responsible for the p.R719W mutation. b Protein alignment of the GTPase effector domain in various dynamins. Mutated residue is colored red