Associated Papers
Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD).
Pinto E Vairo F et al.
Journal of Translational Medicine, 2023
37353797 (PubMed )
Supplement: 12967_2023_4183_MOESM3_ESM.xlsx › Table_S3
Neurological Disorders Associated with WWOX Germline Mutations-A Comprehensive Overview.
Banne E et al.
Cells, 2021
33916893 (PubMed )
Supplement: cells-10-00824-s001.zip › supplementary_materials › Table_2_SuppInfo_Clinvar_Uncertain_significance_variants_that_linked_to_WOREE_and_SCAR12_.xlsx › Uncertain_significance_variants
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