Figure 3 of
Han, Mol Vis 2017; 23:649-659.
Figure 3.
Pedigrees of three patients with mutations in
NMNAT1
. These patients were nonconsanguineous, and all patients harbored a pathogenic mutation in
NMNAT1
(c.709C>T; p. Arg237Cys), which was supposed to be a founder mutation in Koreans.