Noncanonical splice-site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies.
Norifumi KawamotoYuichi HamadaShunsuke KobayashiHiroya NaruseHiroyuki IshiuraTakashi MatsukawaJun MitsuiShoji TsujiMasahiro SonooTatsushi TodaPublished in: Journal of the peripheral nervous system : JPNS (2023)
Searching for sequence variants located outside the canonical splice sites should also be considered even when deletion of PMP22 is not found in a patient with a clinical diagnosis suggesting HNPP.