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Exome Sequencing Reveals a Novel PRPS1 Mutation in a Family with CMTX5 without Optic Atrophy

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Fig. 1. Pedigree, sequencing, and con- con-servation analysis. A: Pedigree of a  Ko-rean family with X-linked  Charcot-Marie-Tooth disease type 5
Table 2. Whole-exome sequencing analysis in the affected indi- indi-vidual

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