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Widening the phenotypical spectrum of EGR2-related CMT: Unusual phenotype for R409W mutation.
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Authors: Leonardi L, Garibaldi M, Fionda L, Vanoli F, Loreti S, Morino S, Antonini G
PMID: 30481651 [PubMed - as supplied by publisher]
from PubMed via alexandrossfakianakis on Inoreader https://ift.tt/2Aw8A1S
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