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
Ectodermal dysplasia with immunodeficiency caused by a branch-point mutation in IKBKG/NEMO.
Jørgensen SE et al.
The Journal of Allergy and Clinical Immunology, 2016
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