Identification of a novel and a recurrent CDC45 variant in a Chinese family with Meier-Gorlin syndrome 7 and a literature review
Front Genet. 2026 Aug 24;17:1893476. doi: 10.3389/fgene.2026.1893476. eCollection 2026. ABSTRACT INTRODUCTION: Meier-Gorlin syndrome 7 (MGORS7) is a rare autosomal recessive disorder characterized by primordial dwarfism, …