Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome

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Authors: Woosub Shin, Martina Kutmon, Eleni Mina, Therese van Amelsvoort, Chris T Evelo, Friederike Ehrhart

Journal title: Orphanet Journal of Rare Diseases

Journal number: 18

Journal publisher: BioMed Central

Published year: 2023

DOI identifier: 10.1186/s13023-023-02953-6

ISSN: 1750-1172