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Stawarski M, Bielopolski N, Roitman I, Fridman K, Wald-Altman S, Eitel M, Hui B, Vulto-van Silfhout A, Stegmann APA, Chirita-Emandi A, Eason J, Bradshaw K, Darnell L, Kostrzewa G, Ploski R, Meurs R, Batté A, Antonarakis SE, Gassmann M, Bettler B.
Stawarski M, et al. Among authors: gassmann m.
NPJ Genom Med. 2026 Mar 9. doi: 10.1038/s41525-026-00558-z. Online ahead of print.
NPJ Genom Med. 2026.
PMID: 41803176
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