Enrichment of mutations in chromatin regulators in people with Rett Syndrome lacking mutations in MECP2
暂无分享,去创建一个
J. Lupski | R. Gibbs | D. Muzny | S. Jhangiani | W. Kaufmann | S. Skinner | M. Friez | S. Sajan | D. Glaze | A. Percy | J. Lane | Samin A Sajan | J. Neul | F. Annese | D. Muzny