Publication | Open Access

Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the “Mowat–Wilson” syndrome

Diverse ExpressionTranscriptional RegulationDevelopmental BiologyDisease MechanismMendelian DisorderGenetic DisorderGeneticsPathologyHuman DevelopmentZfhx1b Gene TranscriptsMolecular MedicineMedicineCell DevelopmentNeurogenetics