Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum.
Sara TaghizadehRaheleh VazehanMaryam BeheshtianFarnaz SadeghiniaZohreh FattahiMarzieh MohseniSanaz ArzhangiShahriar NafissiAriana KariminejadHossein NajmabadiKimia KahriziPublished in: Archives of Iranian medicine (2020)
Our results highlight the advantage of using WES for genetic diagnosis in highly heterogeneous diseases such as IPNs. Moreover, functional analysis is required for novel and uncertain variants.