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 journalArticle

20 Citations (Scopus)

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Medicine & Life Sciences