Publication | Open Access

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

Unusual Intronic MutationsSomatic VariantMendelian DisorderGenetic DisorderGeneticsMolecular BiologyPathologyWerner Syndrome PatientsMolecular GeneticsWrn MutationsDisease Gene IdentificationMedicineClinical Genetics