A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions
Titel:
A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions
Auteur:
Garg, Paras Jadhav, Bharati Rodriguez, Oscar L. Patel, Nihir Martin-Trujillo, Alejandro Jain, Miten Metsu, Sofie Olsen, Hugh Paten, Benedict Ritz, Beate Kooy, R. Frank Gecz, Jozef Sharp, Andrew J.