A Novel Point Mutation in the PMP22 Gene in a Family with Roussy-Levy Syndrome
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Citing Articles
Peripheral Myelin Protein 22 Gene Mutations in Charcot-Marie-Tooth Disease Type 1E Patients.
Jung N, Kwon H, Nam D, Tamanna N, Lee A, Kim S Genes (Basel). 2022; 13(7).
PMID: 35886002 PMC: 9321036. DOI: 10.3390/genes13071219.
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