Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease.

Human molecular genetics
2020
https://researcherprofiles.org/profile/75424200
31625560
Alankarage D, Szot JO, Pachter N, Slavotinek A, Selleri L, Shieh JT, Winlaw D, Giannoulatou E, Chapman G, Dunwoodie SL