Figure 2.
Patients with identified variants, stratified by sequencing method. 100kGP, 100,000 Genomes Project; NIHR RDC, National Institute of Health Research Rare Diseases Consortium; P, pathogenic.

Patients with identified variants, stratified by sequencing method. 100kGP, 100,000 Genomes Project; NIHR RDC, National Institute of Health Research Rare Diseases Consortium; P, pathogenic.

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