Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2.
Marlinde L van den BoogaardP E ThijssenC AytekinF LicciardiA A KıykımL SpossitoV A S H DalmG J DriessenR KersseboomF de VriesM M van Ostaijen-Ten DamA IkinciogullariF DoguM OleastroE BailardoL DaxingerE NainS BarisM J D van TolC WeemaesS M van der MaarelPublished in: Clinical genetics (2017)
Our study expands the mutation spectrum in ICF syndrome and supports that DNMT3B and ZBTB24 are the most common disease genes.