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. 2018 Jul 24;19(4):215–225. doi: 10.1007/s10048-018-0555-7

Fig. 2.

Fig. 2

Pedigrees and electropherograms of five additional Costa Rican CMT families with affected members due to compound heterozygosity for two PNKP variants, the mutated alleles c.1549C>T, found in the large initial family, and the c.1221_1223del, previously related to ataxia with oculomotor apraxia