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- W3206099997 abstract "There is a wide variability of phenotype expression in patients affected with Charcot-Marie-Tooth disease type 1A (CMT1A) but no univocal explanations are available. Single nucleotide polymorphisms (SNPs) could play a role in modulating clinical picture in several conditions but definite evidence regarding CMT1A is missing." @default.
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- W3206099997 date "2021-10-01" @default.
- W3206099997 modified "2023-09-24" @default.
- W3206099997 title "Single nucleotide polymorphisms as possible phenotype modifiers in Charcot-Marie-Tooth 1A disease: A cohort study" @default.
- W3206099997 doi "https://doi.org/10.1016/j.jns.2021.118384" @default.
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