A survey of rare epigenetic variation in 23,116 human genomes identifies disease-relevant epivariations and novel CGG expansions
Authors
Paras Garg,
Bharati JadhavOscar Rodriguez,
Nihir Patel,
Alejandro Martin-Trujillo,
Miten Jain,
Sofie Metsu,
Hugh Olsen,
Benedict Paten,
Beate Ritz,
R Kooy,
Jozef Gecz,
Andrew Sharp,
R. Kooy +12 authors
,
Jozef Gécz Tip Tip