Associated Papers
Oxford Nanopore Technologies [ONT] Sequencing: Clinical Validation in Genetically Heterogeneous Disorders.
Urtis M et al.
Genes, 2025
41300778 (PubMed )
Supplement: genes-16-01325-s001.zip › genes-3897287-supplementary.pdf
Multiple neoplasia in a patient with Gitelman syndrome harboring germline monoallelic MUTYH mutation.
Chan JY et al.
Npj Genomic Medicine, 2020
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