Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome
Published in Orphanet Journal of Rare Diseases, 2023
W. Shin, M. Kutmon, E. Mina, T. van Amelsvoort, C. T. Evelo, F. Ehrhart. (2023). “Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome.” Orphanet Journal of Rare Diseases.
Recommended citation: W. Shin, M. Kutmon, E. Mina, T. van Amelsvoort, C. T. Evelo, F. Ehrhart. (2023). "Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome." Orphanet Journal of Rare Diseases.
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