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Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype
Khalid Al-Thihli, Teresa Rudkin, Nancy Carson, Chantal Poulin, Serge Melançon, Vazken M. Der Kaloustian
Research output: Contribution to journal › Article › peer-review
24
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(Scopus)