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A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsies

✍ Scribed by H. Zéphir; T. Stojkovic; P. Latour; J.F. Hurtevent; F. Blankaert; P. Vermersch

No coin nor oath required. For personal study only.

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