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. 2012 Dec 12;7(12):e51155. doi: 10.1371/journal.pone.0051155

Figure 1. Sequences of mutations detected and family trees of the patients with each base substitution.

Figure 1

(A) Japanese family of MRX214 with Del 312F in GPR37. (B) Caucasian family of AU0654 with mutation R558Q in GPR37. (C) Caucasian family with T589M in GPR37. Closed boxes and circles indicate the individual with ASD, + indicate the individual with mutations.