Primary Site >> Colorectal Cancer

Gene >> ZNF2

Journal: Metabolism. 2017 Jun;71:213-225.
Title: Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome (MDPL).
Author: Elouej, Sahar|Beleza-Meireles, Ana|Caswell, Richard|Colclough, Kevin|Ellard, Sian|Desvignes, Jean Pierre|Beroud, Christophe|Levy, Nicolas|Mohammed, Shehla|De Sandre-Giovannoli, Annachiara
PMID: 28521875