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A survey of rare epigenetic variation in 23,116 human genomes identifies disease-relevant epivariations and novel CGG expansions

Publication

Date: 26th March 2020 | Source: BioRxiv

Authors: Paras Garg, Bharati Jadhav, Oscar L. Rodriguez, Nihir Patel, Alejandro Martin-Trujillo, Miten Jain, Sofie Metsu, Hugh Olsen, Benedict Paten, Beate Ritz, R. Frank Kooy, Jozef Gecz, Andrew J. Sharp.

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