Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleRefining the clinical phenotype associated with missense variants in exons 38 and 39 of KMT2D.AuthorsTharreau, Mylène; Garde, Aurore; Marlin, Sandrine; Morel, Godelieve; Ernest, Sylvain; Nambot, Sophie; Duffourd, Yannis; Ternoy, Ninon; Duvillard, Christian; Banka, Siddharth; Philippe, Christophe; Thauvin‐Robinet, Christel; Mau‐Them, Frederic Tran; Faivre, LaurencePublicationAmerican Journal of Medical Genetics. Part A, 2022, Vol 188, Issue 5, p1600ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.62642