A heterozygous protein‐truncating <i><scp>RFX</scp>6</i> variant in a family with childhood‐onset, pregnancy‐associated and adult‐onset diabetes

Abstract

This study provides supporting evidence for the causal relationship between heterozygous RFX6 mutations and MODY. Furthermore, our results indicate that phenotypic consequences of RFX6 mutations are highly variable even within a single family, and possibly include childhood-onset and pregnancy-associated non-autoimmune diabetes.