Phenotypic similarity-based approach for variant prioritization for unsolved rare disease: a preliminary methodological report
Lagorce, David, Lebreton, Emeline, Matalonga, Leslie, Hongnat, Oscar, Chahdil, Maroua, Piscia, Davide, Paramonov, Ida, Ellwanger, Kornelia, Köhler, Sebastian, Robinson, Peter, Graessner, Holm, Beltran, Sergi, Lucano, Caterina, Hanauer, Marc, Rath, Ana
Published in European journal of human genetics : EJHG (01.02.2024)
Published in European journal of human genetics : EJHG (01.02.2024)
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